A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603908



Internal ID6990939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5753079..5763532hg38UCSC Ensembl
Innerchr5:5753096..5763515hg38UCSC Ensembl
Outerchr5:5753062..5763549hg38UCSC Ensembl
chr5:5753192..5763645hg19UCSC Ensembl
Innerchr5:5753209..5763628hg19UCSC Ensembl
Outerchr5:5753175..5763662hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3810454
hg1910454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11799915
SamplesNA19443
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603908
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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