A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029730



Internal ID21939073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35578306..35579485hg38UCSC Ensembl
chr18:33158270..33159449hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg381180
hg191180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029730
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