A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642339



Internal ID7029109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:41802277..41855882hg38UCSC Ensembl
chr18:39382242..39435847hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3853606
hg1953606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv612e214
Supporting Variantsessv15855554, essv15855555, essv15855552, essv15855553, essv15855556
SamplesNA11829, HG00282, HG00190, HG00366, HG00180
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642339
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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