A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059998



Internal ID21969232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62468012..62468162hg38UCSC Ensembl
chr20:61043068..61043218hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619100
Samples
Known GenesGATA5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059998
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer