A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063385



Internal ID19152604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:15149296..15553893hg38UCSC Ensembl
Innerchr21:16521617..16926212hg19UCSC Ensembl
Innerchr21:15443488..15848083hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38404598
hg19404596
hg18404596
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586461
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)nsv1063385
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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