A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525515



Internal ID15452808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:89921413..89925397hg38UCSC Ensembl
Innerchr6:90631132..90635116hg19UCSC Ensembl
Innerchr6:90687853..90691837hg18UCSC Ensembl
Innerchr6:90687853..90691837hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383985
hg193985
hg183985
hg173985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701648
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525515
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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