A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697228



Internal ID15087194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181148250..181180883hg38UCSC Ensembl
Innerchr5:180575250..180607883hg19UCSC Ensembl
Innerchr5:180507856..180540489hg18UCSC Ensembl
Innerchr5:180507856..180540489hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3832634
hg1932634
hg1832634
hg1732634
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520110
Supporting Variants
Samples
Known GenesOR2V2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697228
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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