A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702131



Internal ID15092097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6017935..6036116hg38UCSC Ensembl
Innerchr10:6059898..6078079hg19UCSC Ensembl
Innerchr10:6099904..6118085hg18UCSC Ensembl
Innerchr10:6099904..6118085hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3818182
hg1918182
hg1818182
hg1718182
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525927
Supporting Variants
Samples
Known GenesIL2RA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702131
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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