A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641777



Internal ID6681859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10451086..10456054hg38UCSC Ensembl
Innerchr18:10451086..10456054hg38UCSC Ensembl
Outerchr18:10450586..10456554hg38UCSC Ensembl
chr18:10451083..10456051hg19UCSC Ensembl
Innerchr18:10451083..10456051hg19UCSC Ensembl
Outerchr18:10450583..10456551hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg384969
hg194969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15804497, essv15804498
SamplesHG00306, NA12004
Known GenesAPCDD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641777
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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