A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993659



Internal ID19237981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:34586124..34601376hg38UCSC Ensembl
Outerchr13:35160261..35175513hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3815253
hg1915253
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1142149
Supporting Variants
SamplesKWS2
Known GenesLINC00457
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993659
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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