A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028978



Internal ID87021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6281068..6281324hg38UCSC Ensembl
chr10:6323031..6323287hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478907
Supporting Variants
Samples
Known GenesLOC399715
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028978
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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