A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643508



Internal ID7030267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4667269..4668064hg38UCSC Ensembl
Innerchr19:4667319..4668014hg38UCSC Ensembl
Outerchr19:4667219..4668114hg38UCSC Ensembl
chr19:4667281..4668076hg19UCSC Ensembl
Innerchr19:4667331..4668026hg19UCSC Ensembl
Outerchr19:4667231..4668126hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15982224
SamplesHG01341
Known GenesC19orf10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643508
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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