A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586167



Internal ID6973687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58573499..58574476hg38UCSC Ensembl
Innerchr1:58573517..58574458hg38UCSC Ensembl
Outerchr1:58573481..58574494hg38UCSC Ensembl
chr1:59039171..59040148hg19UCSC Ensembl
Innerchr1:59039189..59040130hg19UCSC Ensembl
Outerchr1:59039153..59040166hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38978
hg19978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9941822
SamplesNA20822
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586167
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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