A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15991900



Internal ID5993716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12053796..12066895hg38UCSC Ensembl
Innerchr19:12054296..12066395hg38UCSC Ensembl
Outerchr19:12052796..12067895hg38UCSC Ensembl
chr19:12164611..12177710hg19UCSC Ensembl
Innerchr19:12165111..12177210hg19UCSC Ensembl
Outerchr19:12163611..12178710hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3813100
hg1913100
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643692
Supporting Variants
SamplesHG01845
Known GenesZNF844
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15991900
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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