A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16964961



Internal ID43951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9653770..9653821hg38UCSC Ensembl
chr5:9653882..9653933hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5398073
Supporting Variants
Samples
Known GenesLOC285692
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16964961
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002029


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