A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148973



Internal ID18855135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:6055471..6055899hg38UCSC Ensembl
Outerchr10:6097434..6097862hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997760
SamplesKWB1
Known GenesIL2RA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148973
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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