A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15804482



Internal ID509451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10325236..10345901hg38UCSC Ensembl
Innerchr18:10325736..10345401hg38UCSC Ensembl
Outerchr18:10324236..10346901hg38UCSC Ensembl
chr18:10325233..10345898hg19UCSC Ensembl
Innerchr18:10325733..10345398hg19UCSC Ensembl
Outerchr18:10324233..10346898hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3820666
hg1920666
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641773
Supporting Variants
SamplesHG00182
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15804482
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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