A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16107226



Internal ID1836947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57324301..57325114hg38UCSC Ensembl
Innerchr19:57324301..57325114hg38UCSC Ensembl
Outerchr19:57324163..57325238hg38UCSC Ensembl
chr19:57835669..57836482hg19UCSC Ensembl
Innerchr19:57835669..57836482hg19UCSC Ensembl
Outerchr19:57835531..57836606hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38814
hg19814
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644901
Supporting Variants
SamplesHG01705
Known GenesZNF543
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16107226
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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