A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644161



Internal ID7030917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32065127..32066373hg38UCSC Ensembl
Innerchr19:32065135..32066366hg38UCSC Ensembl
Outerchr19:32065120..32066381hg38UCSC Ensembl
chr19:32556033..32557279hg19UCSC Ensembl
Innerchr19:32556041..32557272hg19UCSC Ensembl
Outerchr19:32556026..32557287hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381247
hg191247
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16039966
SamplesHG02722
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644161
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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