A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608341



Internal ID6995271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22886255..22887038hg38UCSC Ensembl
Innerchr6:22886305..22886988hg38UCSC Ensembl
Outerchr6:22886205..22887088hg38UCSC Ensembl
chr6:22886484..22887267hg19UCSC Ensembl
Innerchr6:22886534..22887217hg19UCSC Ensembl
Outerchr6:22886434..22887317hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38784
hg19784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12225818
SamplesHG00107
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608341
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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