A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771900



Internal ID19311984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:29164634..29167835hg38UCSC Ensembl
chr18:26744599..26747800hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg383202
hg193202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076455
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771900
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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