A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141234



Internal ID19276060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:97608846..97611946hg38UCSC Ensembl
Outerchr13:98261100..98264200hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg383101
hg193101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992739
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141234
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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