A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112496



Internal ID18903342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:101200595..101209093hg38UCSC Ensembl
Outerchr11:101071326..101079824hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg388499
hg198499
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3966588
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112496
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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