A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15930777



Internal ID5932593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69876494..69891905hg38UCSC Ensembl
chr18:67543730..67559141hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3815412
hg1915412
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642979
Supporting Variants
SamplesNA06984
Known GenesCD226
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15930777
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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