A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703595



Internal ID15093561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:98491631..98497603hg38UCSC Ensembl
Innerchr10:100251388..100257360hg19UCSC Ensembl
Innerchr10:100241378..100247350hg18UCSC Ensembl
Innerchr10:100241378..100247350hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg385973
hg195973
hg185973
hg175973
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517710
Supporting Variants
Samples
Known GenesHPSE2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703595
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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