A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523761



Internal ID15104368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:1941225..1981831hg38UCSC Ensembl
Innerchr17:1844519..1885125hg19UCSC Ensembl
Innerchr17:1791269..1831875hg18UCSC Ensembl
Innerchr17:1791269..1831875hg17UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3840607
hg1940607
hg1840607
hg1740607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699581
Samples
Known GenesRTN4RL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523761
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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