A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134184



Internal ID18924466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:126863397..126863471hg38UCSC Ensembl
Outerchr11:126733292..126733366hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3971667
SamplesKWS2
Known GenesKIRREL3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134184
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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