A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519094



Internal ID15446387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:90010188..90167439hg38UCSC Ensembl
Innerchr10:91769945..91927196hg19UCSC Ensembl
Innerchr10:91759925..91917176hg18UCSC Ensembl
Innerchr10:91759925..91917176hg17UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38157252
hg19157252
hg18157252
hg17157252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696567
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519094
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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