A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3699593



Internal ID18997874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:82099291..82220901hg38UCSC Ensembl
Innerchr1:82564975..82686585hg19UCSC Ensembl
Innerchr1:82337563..82459173hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38121611
hg19121611
hg18121611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004892
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)nssv3699593
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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