A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699581



Internal ID15089547
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523761
Supporting Variants
Samples
Known GenesRTN4RL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699581
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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