A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705914



Internal ID15442566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132070850..132072825hg38UCSC Ensembl
Innerchr10:133884354..133886329hg19UCSC Ensembl
Innerchr10:133734344..133736319hg18UCSC Ensembl
Innerchr10:133734344..133736319hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381976
hg191976
hg181976
hg171976
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520651
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705914
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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