A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643561



Internal ID6683632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6579137..6581947hg38UCSC Ensembl
Innerchr19:6579302..6581897hg38UCSC Ensembl
Outerchr19:6579017..6582067hg38UCSC Ensembl
chr19:6579148..6581958hg19UCSC Ensembl
Innerchr19:6579313..6581908hg19UCSC Ensembl
Outerchr19:6579028..6582078hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382811
hg192811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15986579, essv15986580, essv15986582, essv15986581
SamplesNA21111, HG03652, HG04098, NA21104
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643561
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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