A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608205



Internal ID6995135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17061721..17063713hg38UCSC Ensembl
Innerchr6:17061758..17063676hg38UCSC Ensembl
Outerchr6:17061684..17063750hg38UCSC Ensembl
chr6:17061952..17063944hg19UCSC Ensembl
Innerchr6:17061989..17063907hg19UCSC Ensembl
Outerchr6:17061915..17063981hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381993
hg191993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12202779
SamplesHG00599
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608205
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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