A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644726



Internal ID6684790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52869727..52878536hg38UCSC Ensembl
Innerchr19:52870227..52878036hg38UCSC Ensembl
Outerchr19:52868727..52879536hg38UCSC Ensembl
chr19:53372980..53381789hg19UCSC Ensembl
Innerchr19:53373480..53381289hg19UCSC Ensembl
Outerchr19:53371980..53382789hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg388810
hg198810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16086656, essv16086657
SamplesNA21098, HG03771
Known GenesZNF320
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644726
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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