A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064198



Internal ID19153417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32102349..33970586hg38UCSC Ensembl
Innerchr16:32113670..33773053hg19UCSC Ensembl
Innerchr16:32021171..33680554hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381868238
hg191659384
hg181659384
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2844n100
Supporting Variantsnssv3716263, nssv3716266, nssv3550270, nssv3716265, nssv3550274, nssv3716264, nssv3550273, nssv3550271, nssv3550272
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)nsv1064198
Frequency
Sample Size11257
Observed Gain7
Observed Loss2
Observed Complex0
Frequencyn/a


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