A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517666



Internal ID15444959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8697962..8700649hg38UCSC Ensembl
Innerchr17:8601280..8603967hg19UCSC Ensembl
Innerchr17:8542005..8544692hg18UCSC Ensembl
Innerchr17:8542005..8544692hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg382688
hg192688
hg182688
hg172688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv652767, nssv657901
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517666
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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