A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643009



Internal ID7029778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71165025..71188685hg38UCSC Ensembl
chr18:68832261..68855921hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3823661
hg1923661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv635e214
Supporting Variantsessv15931758, essv15931760, essv15931757, essv15931759
SamplesNA18874, NA06984, HG03888, NA18853
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643009
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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