A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6304735



Internal ID9282138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38916201..38916947hg38UCSC Ensembl
chr20:37544844..37545590hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2674770
Supporting Variants
SamplesNA18606
Known GenesPPP1R16B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6304735
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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