A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013012



Internal ID21922355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27218058..27218184hg38UCSC Ensembl
chr7:27257677..27257803hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564886
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013012
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