A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520901



Internal ID15448194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:90636182..90636946hg38UCSC Ensembl
Innerchr6:91345901..91346665hg19UCSC Ensembl
Innerchr6:91402622..91403386hg18UCSC Ensembl
Innerchr6:91402622..91403386hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38765
hg19765
hg18765
hg17765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv678624, nssv677249
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520901
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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