A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286663



Internal ID20495881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35461130..35461242hg38UCSC Ensembl
chr6:35428907..35429019hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748278
Supporting Variants
Samples
Known GenesFANCE
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286663
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