A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6393668



Internal ID9371071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146936153..146936697hg38UCSC Ensembl
chr5:146315716..146316260hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664858
Supporting Variants
SamplesNA20510
Known GenesPPP2R2B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6393668
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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