A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15997189



Internal ID5999005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14042961..14045862hg38UCSC Ensembl
Innerchr19:14042999..14045824hg38UCSC Ensembl
Outerchr19:14042923..14045900hg38UCSC Ensembl
chr19:14153773..14156674hg19UCSC Ensembl
Innerchr19:14153811..14156636hg19UCSC Ensembl
Outerchr19:14153735..14156712hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382902
hg192902
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643733
Supporting Variants
SamplesHG02586
Known GenesIL27RA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15997189
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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