A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060456



Internal ID19149675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32619935..33807304hg38UCSC Ensembl
Innerchr16:32631256..33609771hg19UCSC Ensembl
Innerchr16:32538757..33517272hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381187370
hg19978516
hg18978516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2876n100
Supporting Variantsnssv3717196
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)nsv1060456
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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