A curated catalogue of human genomic structural variation

Variant Details

Variant: nsv584961

Internal ID

16372370

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr2:241566780..241567855	hg38	UCSC Ensembl
Inner	chr2:242506195..242507270	hg19	UCSC Ensembl
Inner	chr2:242154868..242155943	hg18	UCSC Ensembl

Cytoband

2q37.3

Allele length

Assembly	Allele length
hg38	1076
hg19	1076
hg18	1076

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

M

Merged Variants

Supporting Variants

nssv934680, nssv934663, nssv934636, nssv934652, nssv934718, nssv934654, nssv934669, nssv934648, nssv934656, nssv934672, nssv934711, nssv934702, nssv934671, nssv934650, nssv934633, nssv934714, nssv934709, nssv934693, nssv934720, nssv934639, nssv934689, nssv934676, nssv934641, nssv934653, nssv934700, nssv934662, nssv934626, nssv934707, nssv934698, nssv934628, nssv934640, nssv934665, nssv934670, nssv934666, nssv934635, nssv934642, nssv934712, nssv934692, nssv934630, nssv934717, nssv934686, nssv934719, nssv934632, nssv934706, nssv934688, nssv934703, nssv934678, nssv934655, nssv934660, nssv934681, nssv934675, nssv934658, nssv934691, nssv934696, nssv934649, nssv934627, nssv934708, nssv934705, nssv934682, nssv934625, nssv934715, nssv934694, nssv934684, nssv934624, nssv934683, nssv934695, nssv934674, nssv934634, nssv934701, nssv934685, nssv934697, nssv934637, nssv934699, nssv934679, nssv934647, nssv934704, nssv934677, nssv934667, nssv934661, nssv934646, nssv934687, nssv934713, nssv934690, nssv934629, nssv934657, nssv934673, nssv934643, nssv934710, nssv934645, nssv934631, nssv934644, nssv934659, nssv934651, nssv934668, nssv934638, nssv934716, nssv934664

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	97
Observed Complex	0
Frequency	n/a