A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15933543



Internal ID4721810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:73211862..73434784hg38UCSC Ensembl
chr18:70879097..71102019hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38222923
hg19222923
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643078
Supporting Variants
SamplesNA06984
Known GenesLOC100505817, LOC400655
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15933543
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