A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980589



Internal ID19204612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:113213066..113214632hg38UCSC Ensembl
Outerchr13:113867380..113868946hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381567
hg191567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143402
Supporting Variants
SamplesKWS1
Known GenesCUL4A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980589
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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