A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689261



Internal ID15425913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1257675..1299208hg38UCSC Ensembl
Innerchr16:1307676..1349209hg19UCSC Ensembl
Innerchr16:1247677..1289210hg18UCSC Ensembl
Innerchr16:1247677..1289210hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3841534
hg1941534
hg1841534
hg1741534
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515770
Supporting Variants
Samples
Known GenesTPSD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689261
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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