A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999181



Internal ID19158717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62953762..62996637hg38UCSC Ensembl
Innerchr3:62939437..62982312hg19UCSC Ensembl
Innerchr3:62914477..62957352hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3842876
hg1942876
hg1842876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3594575
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)nsv999181
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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