A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16964308



Internal ID43514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39511891..39511942hg38UCSC Ensembl
chr5:39511993..39512044hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563818
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16964308
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.009621


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