A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603880



Internal ID6990911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:4554566..4557483hg38UCSC Ensembl
Innerchr5:4554575..4557475hg38UCSC Ensembl
Outerchr5:4554558..4557492hg38UCSC Ensembl
chr5:4554679..4557596hg19UCSC Ensembl
Innerchr5:4554688..4557588hg19UCSC Ensembl
Outerchr5:4554671..4557605hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg382918
hg192918
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11794575, essv11794574
SamplesHG03267, HG02970
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603880
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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