A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031903



Internal ID21941246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58171067..58171168hg38UCSC Ensembl
chr18:55838299..55838400hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634771
Samples
Known GenesNEDD4L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031903
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