A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139838



Internal ID18915958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:108256721..108796820hg38UCSC Ensembl
Outerchr13:108909069..109449168hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38540100
hg19540100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978174
SamplesKWS1
Known GenesMYO16, TNFSF13B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139838
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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