A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11961639



Internal ID367650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:84852625..84907906hg38UCSC Ensembl
Innerchr5:84852629..84907902hg38UCSC Ensembl
Outerchr5:84852621..84907910hg38UCSC Ensembl
chr5:84148443..84203724hg19UCSC Ensembl
Innerchr5:84148447..84203720hg19UCSC Ensembl
Outerchr5:84148439..84203728hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3855282
hg1955282
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3605660
Supporting Variants
SamplesHG00105
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11961639
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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