A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528497



Internal ID15455790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:60479745..60510279hg38UCSC Ensembl
Innerchr10:62239503..62270037hg19UCSC Ensembl
Innerchr10:61909509..61940043hg18UCSC Ensembl
Innerchr10:61909509..61940043hg17UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3830535
hg1930535
hg1830535
hg1730535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705102
Samples
Known GenesANK3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528497
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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