A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686897



Internal ID15423549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36118154..36153146hg38UCSC Ensembl
Innerchr17:34445545..34480526hg19UCSC Ensembl
Innerchr17:31469658..31504639hg18UCSC Ensembl
Innerchr17:31469658..31504639hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3834993
hg1934982
hg1834982
hg1734982
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517262
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686897
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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