A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138273



Internal ID19249979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:111874177..111874382hg38UCSC Ensembl
Outerchr13:112528491..112528696hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983393, nssv3971842
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138273
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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