A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633340



Internal ID6673462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100103635..100106765hg38UCSC Ensembl
Innerchr13:100103685..100106566hg38UCSC Ensembl
Outerchr13:100103546..100106854hg38UCSC Ensembl
chr13:100755889..100759019hg19UCSC Ensembl
Innerchr13:100755939..100758820hg19UCSC Ensembl
Outerchr13:100755800..100759108hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg383131
hg193131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14875754, essv14875756, essv14875755
SamplesHG03844, HG03953, HG04227
Known GenesPCCA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633340
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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