A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111098



Internal ID18923835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:113841555..113841676hg38UCSC Ensembl
Outerchr13:114544528..114544649hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962312
SamplesKWS1
Known GenesGAS6, GAS6-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111098
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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