A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3606377



Internal ID6993313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115967519..115969308hg38UCSC Ensembl
Innerchr5:115967523..115969305hg38UCSC Ensembl
Outerchr5:115967516..115969312hg38UCSC Ensembl
chr5:115303216..115305005hg19UCSC Ensembl
Innerchr5:115303220..115305002hg19UCSC Ensembl
Outerchr5:115303213..115305009hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg381790
hg191790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12030218
SamplesHG01845
Known GenesAQPEP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3606377
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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