A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700307



Internal ID15436959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:57393410..57659912hg38UCSC Ensembl
Innerchr8:58305969..58572471hg19UCSC Ensembl
Innerchr8:58468523..58735025hg18UCSC Ensembl
Innerchr8:58468523..58735025hg17UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38266503
hg19266503
hg18266503
hg17266503
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524390
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700307
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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