A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574680



Internal ID21766723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165754687..165754768hg38UCSC Ensembl
chr6:166168175..166168256hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000668
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17574680
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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