A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641732



Internal ID7028503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9074233..9076901hg38UCSC Ensembl
Innerchr18:9074249..9076886hg38UCSC Ensembl
Outerchr18:9074218..9076917hg38UCSC Ensembl
chr18:9074231..9076899hg19UCSC Ensembl
Innerchr18:9074247..9076884hg19UCSC Ensembl
Outerchr18:9074216..9076915hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg382669
hg192669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15795668
SamplesNA19795
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641732
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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