A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643672



Internal ID6683743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11409466..11411198hg38UCSC Ensembl
Innerchr19:11409516..11411148hg38UCSC Ensembl
Outerchr19:11409416..11411248hg38UCSC Ensembl
chr19:11520142..11521874hg19UCSC Ensembl
Innerchr19:11520192..11521824hg19UCSC Ensembl
Outerchr19:11520092..11521924hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381733
hg191733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15990791, essv15990794, essv15990792, essv15990793
SamplesNA20890, HG03736, NA21112, HG03775
Known GenesRGL3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643672
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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