A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644375



Internal ID6684443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41284927..41291335hg38UCSC Ensembl
Innerchr19:41284939..41291324hg38UCSC Ensembl
Outerchr19:41284916..41291347hg38UCSC Ensembl
chr19:41790832..41797240hg19UCSC Ensembl
Innerchr19:41790844..41797229hg19UCSC Ensembl
Outerchr19:41790821..41797252hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg386409
hg196409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16055751
SamplesHG01861
Known GenesHNRNPUL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644375
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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