A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610355



Internal ID6997272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110309499..110340214hg38UCSC Ensembl
Innerchr6:110309999..110339714hg38UCSC Ensembl
Outerchr6:110308499..110341214hg38UCSC Ensembl
chr6:110630702..110661417hg19UCSC Ensembl
Innerchr6:110631202..110660917hg19UCSC Ensembl
Outerchr6:110629702..110662417hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3830716
hg1930716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12502089
SamplesHG03078
Known GenesMETTL24
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610355
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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