A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668042



Internal ID15404694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125371917..125374932hg38UCSC Ensembl
Innerchr10:127060486..127063501hg19UCSC Ensembl
Innerchr10:127050476..127053491hg18UCSC Ensembl
Innerchr10:127050476..127053491hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383016
hg193016
hg183016
hg173016
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517725
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668042
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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