A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3606360



Internal ID6993296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115182016..115196522hg38UCSC Ensembl
Innerchr5:115182166..115196372hg38UCSC Ensembl
Outerchr5:115181866..115196672hg38UCSC Ensembl
chr5:114517713..114532219hg19UCSC Ensembl
Innerchr5:114517863..114532069hg19UCSC Ensembl
Outerchr5:114517563..114532369hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3814507
hg1914507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12026244
SamplesHG03971
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3606360
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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