A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011957



Internal ID21921300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25658003..25658054hg38UCSC Ensembl
chr6:25658231..25658282hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574710
Samples
Known GenesSCGN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011957
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