A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608204



Internal ID6995134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17053393..17063131hg38UCSC Ensembl
Innerchr6:17053393..17063131hg38UCSC Ensembl
Outerchr6:17053346..17063195hg38UCSC Ensembl
chr6:17053624..17063362hg19UCSC Ensembl
Innerchr6:17053624..17063362hg19UCSC Ensembl
Outerchr6:17053577..17063426hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg389739
hg199739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12202778
SamplesHG01890
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608204
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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