A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15917780



Internal ID3965910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:67077863..67131882hg38UCSC Ensembl
chr18:64745100..64799119hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3854020
hg1954020
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642891
Supporting Variants
SamplesHG03616
Known GenesMIR5011
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15917780
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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