A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608294



Internal ID6995224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20394633..20398219hg38UCSC Ensembl
Innerchr6:20394633..20398219hg38UCSC Ensembl
Outerchr6:20394388..20398437hg38UCSC Ensembl
chr6:20394864..20398450hg19UCSC Ensembl
Innerchr6:20394864..20398450hg19UCSC Ensembl
Outerchr6:20394619..20398668hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383587
hg193587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12218497
SamplesHG00524
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608294
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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