A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960595



Internal ID19207760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:52306465..52337265hg38UCSC Ensembl
Outerchr13:52880600..52911400hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3830801
hg1930801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128682
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960595
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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