A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567808



Internal ID21759851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106498738..106498827hg38UCSC Ensembl
chr6:106946613..106946702hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6007491
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567808
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