A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6149098



Internal ID9364168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:23718763..23811144hg38UCSC Ensembl
chr13:24292902..24385283hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3892382
hg1992382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659554
Supporting Variants
SamplesNA18559
Known GenesMIPEP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6149098
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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