A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660920



Internal ID9927025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37480232..37481678hg38UCSC Ensembl
Outerchr13:37480195..37481728hg38UCSC Ensembl
Innerchr13:38054369..38055815hg19UCSC Ensembl
Outerchr13:38054332..38055865hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381534
hg191534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5520468
SamplesNA19625
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660920
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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