A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067367



Internal ID19156586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32147274..34009022hg38UCSC Ensembl
Innerchr16:32158595..33811489hg19UCSC Ensembl
Innerchr16:32066096..33718990hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381861749
hg191652895
hg181652895
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2844n100
Supporting Variantsnssv3550359, nssv3550358, nssv3550356, nssv3550357
Samples
Known GenesHERC2P4, LOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067367
Frequency
Sample Size11257
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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