A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695508



Internal ID15085474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5959479..5959733hg38UCSC Ensembl
Innerchr10:6001442..6001696hg19UCSC Ensembl
Innerchr10:6041448..6041702hg18UCSC Ensembl
Innerchr10:6041448..6041702hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38255
hg19255
hg18255
hg17255
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519436
Supporting Variants
Samples
Known GenesIL15RA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695508
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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