A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9896483



Internal ID5188911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33059376..33064656hg38UCSC Ensembl
Innerchr1:33059452..33064581hg38UCSC Ensembl
Outerchr1:33059301..33064732hg38UCSC Ensembl
chr1:33524977..33530257hg19UCSC Ensembl
Innerchr1:33525053..33530182hg19UCSC Ensembl
Outerchr1:33524902..33530333hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg385281
hg195281
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585680
Supporting Variants
SamplesNA18610
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9896483
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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