A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704610



Internal ID15441262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:40913201..40915982hg38UCSC Ensembl
Innerchr17:39069453..39072234hg19UCSC Ensembl
Innerchr17:36322979..36325760hg18UCSC Ensembl
Innerchr17:36322979..36325760hg17UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg382782
hg192782
hg182782
hg172782
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528074
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704610
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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