A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659744



Internal ID15049710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:63931077..64001974hg38UCSC Ensembl
Innerchr17:62008437..62079334hg19UCSC Ensembl
Innerchr17:59362169..59433066hg18UCSC Ensembl
Innerchr17:59362169..59433066hg17UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3870898
hg1970898
hg1870898
hg1770898
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517272
Supporting Variants
Samples
Known GenesC17orf72, CD79B, SCN4A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659744
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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