A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644203



Internal ID7030959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34234212..34241449hg38UCSC Ensembl
Innerchr19:34234712..34240949hg38UCSC Ensembl
Outerchr19:34233212..34242449hg38UCSC Ensembl
chr19:34725117..34732354hg19UCSC Ensembl
Innerchr19:34725617..34731854hg19UCSC Ensembl
Outerchr19:34724117..34733354hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg387238
hg197238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16043915
SamplesHG03259
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644203
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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