A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698897



Internal ID15088863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:128091905..128109225hg38UCSC Ensembl
Innerchr10:129890169..129907489hg19UCSC Ensembl
Innerchr10:129780159..129797479hg18UCSC Ensembl
Innerchr10:129780159..129797479hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3817321
hg1917321
hg1817321
hg1717321
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523184
Supporting Variants
Samples
Known GenesMKI67
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698897
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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