A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633477



Internal ID7020286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106910874..106915012hg38UCSC Ensembl
chr13:107563222..107567360hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg384139
hg194139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14890394, essv14890398, essv14890401, essv14890392, essv14890400, essv14890396, essv14890393, essv14890395, essv14890397, essv14890399
SamplesHG04158, HG03785, HG03861, HG04235, HG03643, HG04186, HG03692, HG03870, HG03681, NA20887
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633477
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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