A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050222



Internal ID21959455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51561336..51561393hg38UCSC Ensembl
chr20:50177875..50177932hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635993
Samples
Known GenesNFATC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050222
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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