A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025829



Internal ID21935172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12003469..12006944hg38UCSC Ensembl
chr18:12003468..12006943hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg383476
hg193476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625090
Samples
Known GenesIMPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025829
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