A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705266



Internal ID15095232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5959053..5962049hg38UCSC Ensembl
Innerchr10:6001016..6004012hg19UCSC Ensembl
Innerchr10:6041022..6044018hg18UCSC Ensembl
Innerchr10:6041022..6044018hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg382997
hg192997
hg182997
hg172997
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)nssv705266
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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