A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959952



Internal ID19219439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:15235901..15256001hg38UCSC Ensembl
Outerchr18:15235900..15256000hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3820101
hg1920101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110306
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959952
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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