A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3606376



Internal ID6993312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115919421..115923631hg38UCSC Ensembl
Innerchr5:115919449..115923604hg38UCSC Ensembl
Outerchr5:115919394..115923659hg38UCSC Ensembl
chr5:115255118..115259328hg19UCSC Ensembl
Innerchr5:115255146..115259301hg19UCSC Ensembl
Outerchr5:115255091..115259356hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg384211
hg194211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12030217
SamplesHG02676
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3606376
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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