A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703897



Internal ID15440549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:137045124..137117313hg38UCSC Ensembl
Innerchr8:138057367..138129556hg19UCSC Ensembl
Innerchr8:138126549..138198738hg18UCSC Ensembl
Innerchr8:138126549..138198738hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3872190
hg1972190
hg1872190
hg1772190
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527455
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703897
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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