A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610997



Internal ID6997910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140307702..140397851hg38UCSC Ensembl
chr6:140628839..140718988hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3890150
hg1990150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12568536
SamplesNA19759
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610997
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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