A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019519



Internal ID21928862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164071293..164072035hg38UCSC Ensembl
chr6:164492325..164493067hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38743
hg19743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562634
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019519
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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