A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694272



Internal ID15430924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15724015..15741192hg38UCSC Ensembl
Innerchr17:15627329..15644506hg19UCSC Ensembl
Innerchr17:15568054..15585231hg18UCSC Ensembl
Innerchr17:15568054..15585231hg17UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3817178
hg1917178
hg1817178
hg1717178
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518765
Supporting Variants
Samples
Known GenesTBC1D26
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694272
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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