A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643008



Internal ID7029777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71164021..71187186hg38UCSC Ensembl
Innerchr18:71164521..71186686hg38UCSC Ensembl
Outerchr18:71163021..71188186hg38UCSC Ensembl
chr18:68831257..68854422hg19UCSC Ensembl
Innerchr18:68831757..68853922hg19UCSC Ensembl
Outerchr18:68830257..68855422hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3823166
hg1923166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv635e214
Supporting Variantsessv15931755, essv15931754, essv15931756
SamplesNA06984, HG03888, HG03061
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643008
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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