A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642222



Internal ID7028992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36270024..36276740hg38UCSC Ensembl
Innerchr18:36270037..36276728hg38UCSC Ensembl
Outerchr18:36270012..36276753hg38UCSC Ensembl
chr18:33849987..33856703hg19UCSC Ensembl
Innerchr18:33850000..33856691hg19UCSC Ensembl
Outerchr18:33849975..33856716hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg386717
hg196717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15842429, essv15842427, essv15842428
SamplesHG03851, HG03802, HG03488
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642222
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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