A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525960



Internal ID15453253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4715630..4715926hg38UCSC Ensembl
Innerchr10:4757822..4758118hg19UCSC Ensembl
Innerchr10:4747822..4748118hg18UCSC Ensembl
Innerchr10:4747822..4748118hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38297
hg19297
hg18297
hg17297
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702171
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525960
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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