A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520357



Internal ID15100964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78568229..78577234hg38UCSC Ensembl
Innerchr17:76564311..76573316hg19UCSC Ensembl
Innerchr17:74075906..74084911hg18UCSC Ensembl
Innerchr17:74075906..74084911hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg389006
hg199006
hg189006
hg179006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697370
Samples
Known GenesDNAH17
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520357
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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