A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065498



Internal ID19154717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32499491..33970586hg38UCSC Ensembl
Innerchr16:32510812..33773053hg19UCSC Ensembl
Innerchr16:32418313..33680554hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381471096
hg191262242
hg181262242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2876n100
Supporting Variantsnssv3551822, nssv3551821
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)nsv1065498
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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