A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15931760



Internal ID5337475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71165025..71188685hg38UCSC Ensembl
chr18:68832261..68855921hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3823661
hg1923661
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643009
Supporting Variants
SamplesNA18874
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15931760
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer