A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705070



Internal ID15441722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:109442582..109574206hg38UCSC Ensembl
Innerchr10:111202340..111333964hg19UCSC Ensembl
Innerchr10:111192330..111323954hg18UCSC Ensembl
Innerchr10:111192330..111323954hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38131625
hg19131625
hg18131625
hg17131625
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528468
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705070
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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