A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632184



Internal ID7018994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:56660262..56673570hg38UCSC Ensembl
Innerchr13:56660262..56673570hg38UCSC Ensembl
Outerchr13:56659762..56674070hg38UCSC Ensembl
chr13:57234396..57247704hg19UCSC Ensembl
Innerchr13:57234396..57247704hg19UCSC Ensembl
Outerchr13:57233896..57248204hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3813309
hg1913309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14741403
SamplesHG00530
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632184
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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