A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001297



Internal ID21910640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66901460..66901676hg38UCSC Ensembl
chr7:66366447..66366663hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572122
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001297
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