A curated catalogue of human genomic structural variation

Variant Details

Variant: nsv596054

Internal ID

16036777

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr4:166083189..166083657	hg38	UCSC Ensembl
Inner	chr4:167004341..167004809	hg19	UCSC Ensembl
Inner	chr4:167223791..167224259	hg18	UCSC Ensembl

Cytoband

4q32.3

Allele length

Assembly	Allele length
hg38	469
hg19	469
hg18	469

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

M

Merged Variants

Supporting Variants

nssv1012569, nssv1012669, nssv1012610, nssv1012675, nssv1012663, nssv1012648, nssv1012666, nssv1012699, nssv1012642, nssv1012712, nssv1012606, nssv1012581, nssv1012584, nssv1012709, nssv1012680, nssv1012698, nssv1012634, nssv1012691, nssv1012687, nssv1012617, nssv1012672, nssv1012612, nssv1012704, nssv1012613, nssv1012668, nssv1012589, nssv1012619, nssv1012575, nssv1012635, nssv1012579, nssv1012640, nssv1012614, nssv1012694, nssv1012627, nssv1012713, nssv1012674, nssv1012563, nssv1012653, nssv1012629, nssv1012682, nssv1012624, nssv1012688, nssv1012643, nssv1012637, nssv1012693, nssv1012676, nssv1012633, nssv1012692, nssv1012703, nssv1012644, nssv1012705, nssv1012662, nssv1012659, nssv1012632, nssv1012616, nssv1012560, nssv1012583, nssv1012641, nssv1012607, nssv1012598, nssv1012671, nssv1012665, nssv1012647, nssv1012636, nssv1012639, nssv1012595, nssv1012690, nssv1012603, nssv1012623, nssv1012649, nssv1012593, nssv1012577, nssv1012572, nssv1012645, nssv1012590, nssv1012561, nssv1012622, nssv1012715, nssv1012714, nssv1012689, nssv1012670, nssv1012599, nssv1012618, nssv1012651, nssv1012588, nssv1012686, nssv1012708, nssv1012578, nssv1012696, nssv1012683, nssv1012609, nssv1012591, nssv1012568, nssv1012615, nssv1012594, nssv1012664, nssv1012601, nssv1012646, nssv1012621, nssv1012661, nssv1012678, nssv1012597, nssv1012685, nssv1012567, nssv1012658, nssv1012654, nssv1012608, nssv1012586, nssv1012626, nssv1012559, nssv1012677, nssv1012630, nssv1012625, nssv1012681, nssv1012697, nssv1012576, nssv1012574, nssv1012570, nssv1012605, nssv1012660, nssv1012655, nssv1012580, nssv1012596, nssv1012587, nssv1012650, nssv1012701, nssv1012684, nssv1012620, nssv1012600, nssv1012667, nssv1012657, nssv1012604, nssv1012710, nssv1012582, nssv1012628, nssv1012716, nssv1012566, nssv1012700, nssv1012711, nssv1012707, nssv1012585, nssv1012571, nssv1012706, nssv1012631, nssv1012695, nssv1012638, nssv1012673, nssv1012611, nssv1012702, nssv1012652, nssv1012602, nssv1012573, nssv1012679, nssv1012564, nssv1012562, nssv1012592, nssv1012565, nssv1012656

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	158
Observed Complex	0
Frequency	n/a