A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603899



Internal ID6990930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5375569..5378267hg38UCSC Ensembl
Innerchr5:5375576..5378261hg38UCSC Ensembl
Outerchr5:5375563..5378274hg38UCSC Ensembl
chr5:5375682..5378380hg19UCSC Ensembl
Innerchr5:5375689..5378374hg19UCSC Ensembl
Outerchr5:5375676..5378387hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg382699
hg192699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11797704, essv11797703, essv11797702
SamplesNA20787, NA12778, HG01678
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603899
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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