A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15812835



Internal ID2110317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14063029..14098929hg38UCSC Ensembl
chr18:14063028..14098928hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3835901
hg1935901
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641871
Supporting Variants
SamplesHG01920
Known GenesZNF519
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15812835
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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