A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670676



Internal ID9936781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:23772537..24054444hg38UCSC Ensembl
chr19:23955339..24237246hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38281908
hg19281908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6015093
SamplesNA20542
Known GenesRPSAP58, ZNF254, ZNF726
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670676
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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