A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515910



Internal ID15442967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:74175031..74242632hg38UCSC Ensembl
Innerchr8:75087266..75154867hg19UCSC Ensembl
Innerchr8:75249820..75317421hg18UCSC Ensembl
Innerchr8:75249820..75317421hg17UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3867602
hg1967602
hg1867602
hg1767602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700210, nssv684495, nssv665255
Samples
Known GenesJPH1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515910
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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