A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643563



Internal ID6683634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6657080..6660695hg38UCSC Ensembl
Innerchr19:6657097..6660679hg38UCSC Ensembl
Outerchr19:6657064..6660712hg38UCSC Ensembl
chr19:6657091..6660706hg19UCSC Ensembl
Innerchr19:6657108..6660690hg19UCSC Ensembl
Outerchr19:6657075..6660723hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383616
hg193616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15986608, essv15986607
SamplesHG03297, HG03168
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643563
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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