A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3732672



Internal ID19030953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18998986..19025379hg38UCSC Ensembl
Innerchr21:20371304..20397698hg19UCSC Ensembl
Innerchr21:19293175..19319569hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3826394
hg1926395
hg1826395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063400
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)nssv3732672
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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