A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3952494



Internal ID21372563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5962341..5962670hg38UCSC Ensembl
chr20:5942987..5943316hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15179335
SamplesHG002
Known GenesMCM8
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3952494
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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