A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3604062



Internal ID6991092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:13202777..13338409hg38UCSC Ensembl
Innerchr5:13202794..13338393hg38UCSC Ensembl
Outerchr5:13202761..13338426hg38UCSC Ensembl
chr5:13202889..13338521hg19UCSC Ensembl
Innerchr5:13202906..13338505hg19UCSC Ensembl
Outerchr5:13202873..13338538hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38135633
hg19135633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11817727
SamplesNA12234
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3604062
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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