A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16049694



Internal ID2611883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36538069..36560886hg38UCSC Ensembl
Innerchr19:36538069..36560886hg38UCSC Ensembl
Outerchr19:36537569..36561386hg38UCSC Ensembl
chr19:37028971..37051788hg19UCSC Ensembl
Innerchr19:37028971..37051788hg19UCSC Ensembl
Outerchr19:37028471..37052288hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3822818
hg1922818
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644264
Supporting Variants
SamplesHG02314
Known GenesZNF529
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16049694
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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