A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976823



Internal ID51934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177625445..177626293hg38UCSC Ensembl
chr5:177052446..177053294hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38849
hg19849
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456714
Supporting Variants
Samples
Known GenesLOC202181
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976823
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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