A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065815



Internal ID19155034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32102349..32632041hg38UCSC Ensembl
Innerchr16:32113670..32643362hg19UCSC Ensembl
Innerchr16:32021171..32550863hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38529693
hg19529693
hg18529693
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2848n100
Supporting Variantsnssv3550255, nssv3716255, nssv3716256
Samples
Known GenesHERC2P4, LOC390705, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065815
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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