A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978706



Internal ID53180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:175612409..175637270hg38UCSC Ensembl
chr5:175039412..175064273hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3824862
hg1924862
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462927
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978706
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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