A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729213



Internal ID19027494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:117211492..117372603hg38UCSC Ensembl
Innerchr2:117969068..118130179hg19UCSC Ensembl
Innerchr2:117685538..117846649hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38161112
hg19161112
hg18161112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011331
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)nssv3729213
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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