A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527269



Internal ID15454562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81359454..81374678hg38UCSC Ensembl
Innerchr10:83119210..83134434hg19UCSC Ensembl
Innerchr10:83109190..83124414hg18UCSC Ensembl
Innerchr10:83109190..83124414hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3815225
hg1915225
hg1815225
hg1715225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703678
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527269
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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