A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134994



Internal ID18923665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:113935143..113935461hg38UCSC Ensembl
Outerchr11:113805865..113806183hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv724n106
Supporting Variantsnssv3988536
SamplesKWS2
Known GenesHTR3B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134994
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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