A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516035



Internal ID15443092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:95196498..95223223hg38UCSC Ensembl
Innerchr8:96208726..96235451hg19UCSC Ensembl
Innerchr8:96277902..96304627hg18UCSC Ensembl
Innerchr8:96277902..96304627hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3826726
hg1926726
hg1826726
hg1726726
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704862, nssv693651, nssv665851
Samples
Known GenesC8orf69
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516035
Frequency
Sample Size2026
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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