A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978061



Internal ID52780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6649942..6650362hg38UCSC Ensembl
chr6:6650175..6650595hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456735
Supporting Variants
Samples
Known GenesLY86
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978061
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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