A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3604476



Internal ID6991504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:27542840..27579422hg38UCSC Ensembl
Innerchr5:27542856..27579407hg38UCSC Ensembl
Outerchr5:27542825..27579438hg38UCSC Ensembl
chr5:27542947..27579529hg19UCSC Ensembl
Innerchr5:27542963..27579514hg19UCSC Ensembl
Outerchr5:27542932..27579545hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3836583
hg1936583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11848934
SamplesHG01840
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3604476
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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