A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703034



Internal ID15439686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:45892686..46348381hg38UCSC Ensembl
Innerchr5:45892788..46348483hg19UCSC Ensembl
Innerchr5:45928545..46384240hg18UCSC Ensembl
Innerchr5:45928545..46384240hg17UCSC Ensembl
Cytoband5p11
Allele length
AssemblyAllele length
hg38455696
hg19455696
hg18455696
hg17455696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526696
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703034
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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