A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3606399



Internal ID6993335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:116314197..116381855hg38UCSC Ensembl
chr5:115649894..115717552hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3867659
hg1967659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1130e214
Supporting Variantsessv12030560, essv12030562, essv12030561
SamplesHG03770, NA19083, HG04023
Known GenesLOC101927190
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3606399
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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