A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663363



Internal ID9582782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56184064..56213899hg38UCSC Ensembl
Outerchr19:56184027..56213949hg38UCSC Ensembl
Innerchr19:56695433..56725268hg19UCSC Ensembl
Outerchr19:56695396..56725318hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3829923
hg1929923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5904260
SamplesHG00473
Known GenesGALP, ZSCAN5B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663363
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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