A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641597



Internal ID6681682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3389935..3421195hg38UCSC Ensembl
chr18:3389933..3421193hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3831261
hg1931261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15779332
SamplesHG03937
Known GenesTGIF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641597
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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