A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699714



Internal ID15436366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36118154..36137569hg38UCSC Ensembl
Innerchr17:34445545..34464949hg19UCSC Ensembl
Innerchr17:31469658..31489062hg18UCSC Ensembl
Innerchr17:31469658..31489062hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3819416
hg1919405
hg1819405
hg1719405
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)nssv699714
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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