A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692418



Internal ID15082384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5959053..5966650hg38UCSC Ensembl
Innerchr10:6001016..6008613hg19UCSC Ensembl
Innerchr10:6041022..6048619hg18UCSC Ensembl
Innerchr10:6041022..6048619hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg387598
hg197598
hg187598
hg177598
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)nssv692418
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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