A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979692



Internal ID53839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15207455..15225024hg38UCSC Ensembl
chr6:15207686..15225255hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3817570
hg1917570
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467285
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979692
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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