A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644176



Internal ID7030932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32682400..32683899hg38UCSC Ensembl
Innerchr19:32682450..32683849hg38UCSC Ensembl
Outerchr19:32682350..32683949hg38UCSC Ensembl
chr19:33173306..33174805hg19UCSC Ensembl
Innerchr19:33173356..33174755hg19UCSC Ensembl
Outerchr19:33173256..33174855hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16041333, essv16041334
SamplesNA19917, HG03127
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644176
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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