A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611055



Internal ID6997966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:141572169..141713116hg38UCSC Ensembl
Innerchr6:141572169..141713116hg38UCSC Ensembl
Outerchr6:141571669..141713616hg38UCSC Ensembl
chr6:141893306..142034253hg19UCSC Ensembl
Innerchr6:141893306..142034253hg19UCSC Ensembl
Outerchr6:141892806..142034753hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38140948
hg19140948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12573193
SamplesHG03716
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611055
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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