A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699536



Internal ID15089502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:18659407..19014011hg38UCSC Ensembl
Innerchr17:18562720..18917324hg19UCSC Ensembl
Innerchr17:18503445..18858049hg18UCSC Ensembl
Innerchr17:18503445..18858049hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38354605
hg19354605
hg18354605
hg17354605
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523721
Supporting Variants
Samples
Known GenesFAM83G, FBXW10, FOXO3B, PRPSAP2, SLC5A10, TRIM16L, TVP23B, ZNF286B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699536
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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