A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960621



Internal ID18868993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:113802527..113803627hg38UCSC Ensembl
Outerchr13:114505500..114506600hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128708
Supporting Variants
SamplesKWS1
Known GenesTMEM255B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960621
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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