A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643804



Internal ID7030561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16800689..16804656hg38UCSC Ensembl
Innerchr19:16800711..16804634hg38UCSC Ensembl
Outerchr19:16800667..16804678hg38UCSC Ensembl
chr19:16911500..16915467hg19UCSC Ensembl
Innerchr19:16911522..16915445hg19UCSC Ensembl
Outerchr19:16911478..16915489hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg383968
hg193968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16002866
SamplesNA20876
Known GenesNWD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643804
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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