A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729384



Internal ID18680979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240320793..240411537hg38UCSC Ensembl
Innerchr2:241260210..241350954hg19UCSC Ensembl
Innerchr2:240908883..240999627hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3890745
hg1990745
hg1890745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008923
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)nssv3729384
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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