A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142149



Internal ID19269065
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 StatusM
Merged Variants
Supporting Variantsnssv3993659
SamplesKWS2
Known GenesLINC00457
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142149
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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