A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520868



Internal ID15448161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70893881..70894004hg38UCSC Ensembl
Innerchr10:72653638..72653761hg19UCSC Ensembl
Innerchr10:72323644..72323767hg18UCSC Ensembl
Innerchr10:72323644..72323767hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38124
hg19124
hg18124
hg17124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697658
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520868
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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