A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15986096



Internal ID5987912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6369167..6370274hg38UCSC Ensembl
Innerchr19:6369218..6370223hg38UCSC Ensembl
Outerchr19:6369116..6370325hg38UCSC Ensembl
chr19:6369178..6370285hg19UCSC Ensembl
Innerchr19:6369229..6370234hg19UCSC Ensembl
Outerchr19:6369127..6370336hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381108
hg191108
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643554
Supporting Variants
SamplesNA18526
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15986096
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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