A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608283



Internal ID6995213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19865001..19867308hg38UCSC Ensembl
Innerchr6:19865001..19867308hg38UCSC Ensembl
Outerchr6:19864795..19867530hg38UCSC Ensembl
chr6:19865232..19867539hg19UCSC Ensembl
Innerchr6:19865232..19867539hg19UCSC Ensembl
Outerchr6:19865026..19867761hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382308
hg192308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12215647
SamplesHG00278
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608283
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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