A curated catalogue of human genomic structural variation

Variant Details

Variant: nsv595229

Internal ID

16382638

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr4:115007591..115008123	hg38	UCSC Ensembl
Inner	chr4:115928747..115929279	hg19	UCSC Ensembl
Inner	chr4:116148196..116148728	hg18	UCSC Ensembl

Cytoband

4q26

Allele length

Assembly	Allele length
hg38	533
hg19	533
hg18	533

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

M

Merged Variants

Supporting Variants

nssv1005665, nssv1005608, nssv1005614, nssv1005672, nssv1005631, nssv1005552, nssv1005494, nssv1005581, nssv1005557, nssv1005627, nssv1005550, nssv1005669, nssv1005516, nssv1005554, nssv1005534, nssv1005599, nssv1005561, nssv1005560, nssv1005642, nssv1005526, nssv1005577, nssv1005634, nssv1005616, nssv1005555, nssv1005686, nssv1005689, nssv1005508, nssv1005596, nssv1005589, nssv1005626, nssv1005645, nssv1005629, nssv1005610, nssv1005495, nssv1005674, nssv1005571, nssv1005656, nssv1005647, nssv1005604, nssv1005582, nssv1005551, nssv1005540, nssv1005541, nssv1005677, nssv1005505, nssv1005547, nssv1005646, nssv1005640, nssv1005638, nssv1005569, nssv1005529, nssv1005639, nssv1005655, nssv1005637, nssv1005632, nssv1005536, nssv1005562, nssv1005593, nssv1005500, nssv1005498, nssv1005641, nssv1005563, nssv1005542, nssv1005549, nssv1005654, nssv1005531, nssv1005620, nssv1005548, nssv1005605, nssv1005685, nssv1005590, nssv1005650, nssv1005617, nssv1005568, nssv1005643, nssv1005588, nssv1005530, nssv1005621, nssv1005532, nssv1005527, nssv1005587, nssv1005683, nssv1005533, nssv1005525, nssv1005538, nssv1005601, nssv1005506, nssv1005513, nssv1005635, nssv1005628, nssv1005622, nssv1005666, nssv1005517, nssv1005574, nssv1005573, nssv1005545, nssv1005648, nssv1005613, nssv1005594, nssv1005612, nssv1005567, nssv1005546, nssv1005522, nssv1005520, nssv1005504, nssv1005496, nssv1005586, nssv1005570, nssv1005658, nssv1005609, nssv1005503, nssv1005595, nssv1005556, nssv1005575, nssv1005611, nssv1005657, nssv1005680, nssv1005572, nssv1005673, nssv1005521, nssv1005502, nssv1005535, nssv1005499, nssv1005510, nssv1005678, nssv1005681, nssv1005663, nssv1005660, nssv1005523, nssv1005661, nssv1005679, nssv1005579, nssv1005492, nssv1005578, nssv1005633, nssv1005671, nssv1005651, nssv1005668, nssv1005653, nssv1005607, nssv1005515, nssv1005512, nssv1005690, nssv1005592, nssv1005615, nssv1005544, nssv1005514, nssv1005511, nssv1005580, nssv1005602, nssv1005652, nssv1005625, nssv1005518, nssv1005537, nssv1005624, nssv1005543, nssv1005659, nssv1005606, nssv1005591, nssv1005583, nssv1005509, nssv1005585, nssv1005493, nssv1005598, nssv1005559, nssv1005676, nssv1005564, nssv1005576, nssv1005636, nssv1005507, nssv1005630, nssv1005565, nssv1005688, nssv1005670, nssv1005584, nssv1005519, nssv1005497, nssv1005687, nssv1005682, nssv1005662, nssv1005684, nssv1005524, nssv1005675, nssv1005600, nssv1005623, nssv1005649, nssv1005597, nssv1005528, nssv1005553, nssv1005667, nssv1005539, nssv1005501, nssv1005618, nssv1005603, nssv1005566, nssv1005558, nssv1005664, nssv1005644, nssv1005619

Samples

Known Genes

Method

SNP array

Analysis

Illumina SNP array copy number analysis

Platform

Not reported

Comments

Reference

Cooper_et_al_2011

Pubmed ID

Accession Number(s)

Frequency

Sample Size	17421
Observed Gain	0
Observed Loss	199
Observed Complex	0
Frequency	n/a