A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955084



Internal ID18858230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:6055483..6055920hg38UCSC Ensembl
Outerchr10:6097446..6097883hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127396
Supporting Variants
SamplesKWS1
Known GenesIL2RA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955084
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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