A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16895316



Internal ID171057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:501968..517000hg38UCSC Ensembl
chr5:180728447..180743984hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3815033
hg1915538
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138370
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16895316
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.025398


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