A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138240



Internal ID19268928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:82315059..82315402hg38UCSC Ensembl
Outerchr13:82889194..82889537hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3971821, nssv3995574
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138240
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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