A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269951



Internal ID20479169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134396077..134396168hg38UCSC Ensembl
chr6:134717215..134717306hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735268
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269951
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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