A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729259



Internal ID19027540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:146844216..146920208hg38UCSC Ensembl
Innerchr2:147601784..147677776hg19UCSC Ensembl
Innerchr2:147318254..147394246hg18UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3875993
hg1975993
hg1875993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001276
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3729259
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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