A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143111



Internal ID19252789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:173399527..173399667hg38UCSC Ensembl
Outerchr4:174320678..174320818hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962585, nssv3984031
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143111
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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