A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984644



Internal ID57145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74744526..75075205hg38UCSC Ensembl
chr6:75454242..75784921hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38330680
hg19330680
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469531
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984644
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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