A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056375



Internal ID19145594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32169453..33908301hg38UCSC Ensembl
Innerchr16:32180774..33710768hg19UCSC Ensembl
Innerchr16:32088275..33618269hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381738849
hg191529995
hg181529995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2842n100
Supporting Variantsnssv3550386, nssv3550385
Samples
Known GenesLOC390705, 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)nsv1056375
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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