A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3619882



Internal ID18918163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19931251..20012082hg38UCSC Ensembl
Innerchr4:19932874..20013705hg19UCSC Ensembl
Innerchr4:19541972..19622803hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3880832
hg1980832
hg1880832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005430
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)nssv3619882
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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