A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134150



Internal ID19266312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:67997212..67997264hg38UCSC Ensembl
Outerchr11:67764683..67764735hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3968689, nssv3985583
SamplesKWS2, KWS1
Known GenesUNC93B1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134150
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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