A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15967980



Internal ID5969796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:982574..993901hg38UCSC Ensembl
chr19:982574..993900hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3811328
hg1911327
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643380
Supporting Variants
SamplesHG01859
Known GenesWDR18
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15967980
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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