A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608295



Internal ID6995225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20463701..20466493hg38UCSC Ensembl
Innerchr6:20463701..20466493hg38UCSC Ensembl
Outerchr6:20463584..20466614hg38UCSC Ensembl
chr6:20463932..20466724hg19UCSC Ensembl
Innerchr6:20463932..20466724hg19UCSC Ensembl
Outerchr6:20463815..20466845hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382793
hg192793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12218498
SamplesNA06984
Known GenesE2F3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608295
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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