A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063520



Internal ID19152739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35237438..35484929hg38UCSC Ensembl
Innerchr16:34471809..34719300hg19UCSC Ensembl
Innerchr16:34329310..34576801hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38247492
hg19247492
hg18247492
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3558709, nssv3558710, nssv3558711
Samples
Known GenesLOC146481, LOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063520
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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