A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518767



Internal ID15446060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11606952..11613715hg38UCSC Ensembl
Innerchr16:11700808..11707571hg19UCSC Ensembl
Innerchr16:11608309..11615072hg18UCSC Ensembl
Innerchr16:11608309..11615072hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg386764
hg196764
hg186764
hg176764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696216
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518767
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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