A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977679



Internal ID52507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177875162..177883324hg38UCSC Ensembl
chr5:177302163..177310325hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg388163
hg198163
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140912
Supporting Variants
Samples
Known GenesLOC728554
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977679
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000208


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