A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008237



Internal ID21917580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150610555..150611898hg38UCSC Ensembl
chr6:150931691..150933034hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381344
hg191344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558127
Samples
Known GenesPLEKHG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008237
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