A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966052



Internal ID18877705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:113802582..113803662hg38UCSC Ensembl
Outerchr13:114505555..114506635hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130143
Supporting Variants
SamplesKWS1
Known GenesTMEM255B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966052
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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