A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997328



Internal ID19156866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:81850349..81932788hg38UCSC Ensembl
Innerchr2:82077473..82159912hg19UCSC Ensembl
Innerchr2:81930984..82013423hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3882440
hg1982440
hg1882440
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582132
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)nsv997328
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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