A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697792



Internal ID15434444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:62664987..62692442hg38UCSC Ensembl
Innerchr17:60742348..60769803hg19UCSC Ensembl
Innerchr17:58096080..58123535hg18UCSC Ensembl
Innerchr17:58096080..58123535hg17UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3827456
hg1927456
hg1827456
hg1727456
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516921
Supporting Variants
Samples
Known GenesMRC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697792
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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