A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003726



Internal ID21913069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40491508..40491699hg38UCSC Ensembl
chr6:40459247..40459438hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570744
Samples
Known GenesLRFN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003726
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