A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15949337



Internal ID4721668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78200644..78304439hg38UCSC Ensembl
chr18:75960644..76064439hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38103796
hg19103796
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643246
Supporting Variants
SamplesNA06984
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15949337
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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