A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129886



Internal ID18936895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:6055438..6055906hg38UCSC Ensembl
Outerchr10:6097401..6097869hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv352n106
Supporting Variantsnssv3965022
SamplesKWS2
Known GenesIL2RA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129886
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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