A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139696



Internal ID19279066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:24330398..24412198hg38UCSC Ensembl
Outerchr19:24513200..24595000hg19UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg3881801
hg1981801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977282
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139696
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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