A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143402



Internal ID19249861
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 StatusM
Merged Variants
Supporting Variantsnssv3980589
SamplesKWS1
Known GenesCUL4A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143402
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer