A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704862



Internal ID15441514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:95203076..95223223hg38UCSC Ensembl
Innerchr8:96215304..96235451hg19UCSC Ensembl
Innerchr8:96284480..96304627hg18UCSC Ensembl
Innerchr8:96284480..96304627hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3820148
hg1920148
hg1820148
hg1720148
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516035
Supporting Variants
Samples
Known GenesC8orf69
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704862
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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