A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610391



Internal ID6997308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112296695..112300753hg38UCSC Ensembl
Innerchr6:112296697..112300751hg38UCSC Ensembl
Outerchr6:112296693..112300755hg38UCSC Ensembl
chr6:112617897..112621955hg19UCSC Ensembl
Innerchr6:112617899..112621953hg19UCSC Ensembl
Outerchr6:112617895..112621957hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384059
hg194059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12505689
SamplesHG02464
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610391
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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