A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586205



Internal ID6973725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60455778..60456272hg38UCSC Ensembl
Innerchr1:60455828..60456222hg38UCSC Ensembl
Outerchr1:60455728..60456322hg38UCSC Ensembl
chr1:60921450..60921944hg19UCSC Ensembl
Innerchr1:60921500..60921894hg19UCSC Ensembl
Outerchr1:60921400..60921994hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9945906
SamplesNA20522
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586205
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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