A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15931755



Internal ID4353733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71164021..71187186hg38UCSC Ensembl
Innerchr18:71164521..71186686hg38UCSC Ensembl
Outerchr18:71163021..71188186hg38UCSC Ensembl
chr18:68831257..68854422hg19UCSC Ensembl
Innerchr18:68831757..68853922hg19UCSC Ensembl
Outerchr18:68830257..68855422hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3823166
hg1923166
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643008
Supporting Variants
SamplesHG03888
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15931755
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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