A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643651



Internal ID6683722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10281270..10282086hg38UCSC Ensembl
Innerchr19:10281320..10282036hg38UCSC Ensembl
Outerchr19:10281220..10282136hg38UCSC Ensembl
chr19:10391946..10392762hg19UCSC Ensembl
Innerchr19:10391996..10392712hg19UCSC Ensembl
Outerchr19:10391896..10392812hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15990330
SamplesNA18978
Known GenesICAM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643651
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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