A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3717185



Internal ID19015466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32513445..33807304hg38UCSC Ensembl
Innerchr16:32524766..33609771hg19UCSC Ensembl
Innerchr16:32432267..33517272hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381293860
hg191085006
hg181085006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056115
Supporting Variants
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3717185
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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