A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526085



Internal ID15453378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105330171..105535424hg38UCSC Ensembl
Innerchr10:107089929..107295182hg19UCSC Ensembl
Innerchr10:107079919..107285172hg18UCSC Ensembl
Innerchr10:107079919..107285172hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38205254
hg19205254
hg18205254
hg17205254
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702329
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526085
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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