A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015756



Internal ID21925099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54685815..54685878hg38UCSC Ensembl
chr6:54550613..54550676hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573909
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015756
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