A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582515



Internal ID16369924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:98239034..98269462hg38UCSC Ensembl
Innerchr2:98855497..98885925hg19UCSC Ensembl
Innerchr2:98221929..98252357hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3830429
hg1930429
hg1830429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv914145
Samples
Known GenesVWA3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582515
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer