A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011134



Internal ID21920477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99803111..99804508hg38UCSC Ensembl
chr7:99400734..99402131hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381398
hg191398
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558556
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011134
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer