A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666201



Internal ID15402853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:123460305..123465997hg38UCSC Ensembl
Innerchr10:125219821..125225513hg19UCSC Ensembl
Innerchr10:125209811..125215503hg18UCSC Ensembl
Innerchr10:125209811..125215503hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg385693
hg195693
hg185693
hg175693
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517588
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666201
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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