A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16964290



Internal ID43501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39334271..39334543hg38UCSC Ensembl
chr5:39334373..39334645hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140813
Supporting Variants
Samples
Known GenesC9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16964290
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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