A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6121621



Internal ID9691144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34781160..34783505hg38UCSC Ensembl
chr13:35355297..35357642hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg382346
hg192346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658240
Supporting Variants
SamplesNA19440
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6121621
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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