A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978063



Internal ID52781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6661362..6661432hg38UCSC Ensembl
chr6:6661595..6661665hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141239
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978063
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.021952


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