A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633329



Internal ID7020138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99429069..99430205hg38UCSC Ensembl
Innerchr13:99429121..99430153hg38UCSC Ensembl
Outerchr13:99429017..99430257hg38UCSC Ensembl
chr13:100081323..100082459hg19UCSC Ensembl
Innerchr13:100081375..100082407hg19UCSC Ensembl
Outerchr13:100081271..100082511hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg381137
hg191137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14873060, essv14873058, essv14873059, essv14873061
SamplesHG02642, HG02882, HG02879, HG03054
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633329
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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