A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698322



Internal ID15434974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:58631618..58631756hg38UCSC Ensembl
Innerchr17:56708979..56709117hg19UCSC Ensembl
Innerchr17:54063978..54064116hg18UCSC Ensembl
Innerchr17:54063978..54064116hg17UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38139
hg19139
hg18139
hg17139
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515871
Supporting Variants
Samples
Known GenesTEX14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698322
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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