A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520692



Internal ID15447985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69512262..69512378hg38UCSC Ensembl
Innerchr10:71272018..71272134hg19UCSC Ensembl
Innerchr10:70942024..70942140hg18UCSC Ensembl
Innerchr10:70942024..70942140hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38117
hg19117
hg18117
hg17117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697560
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520692
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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