A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987282



Internal ID58960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74464441..74465182hg38UCSC Ensembl
chr6:75174157..75174898hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454824
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987282
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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