A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138085



Internal ID19278868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:126301173..126301234hg38UCSC Ensembl
Outerchr11:126171068..126171129hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990628
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138085
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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