A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016293



Internal ID21925636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42840297..42845928hg38UCSC Ensembl
chr6:42808035..42813666hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg385632
hg195632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561482
Samples
Known GenesGLTSCR1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016293
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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