A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641789



Internal ID7028560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11177194..11178270hg38UCSC Ensembl
Innerchr18:11177235..11178229hg38UCSC Ensembl
Outerchr18:11177153..11178311hg38UCSC Ensembl
chr18:11177193..11178269hg19UCSC Ensembl
Innerchr18:11177234..11178228hg19UCSC Ensembl
Outerchr18:11177152..11178310hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381077
hg191077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15805290, essv15805291
SamplesHG00982, HG02079
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641789
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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