A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568975



Internal ID21761018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108264298..108264353hg38UCSC Ensembl
chr6:108585502..108585557hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011542
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568975
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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