A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673898



Internal ID15410550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6194574..6219830hg38UCSC Ensembl
Innerchr17:6097894..6123150hg19UCSC Ensembl
Innerchr17:6038618..6063874hg18UCSC Ensembl
Innerchr17:6038618..6063874hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3825257
hg1925257
hg1825257
hg1725257
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517031
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673898
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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