A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16964965



Internal ID43954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9718840..9719680hg38UCSC Ensembl
chr5:9718952..9719792hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38841
hg19841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468195
Supporting Variants
Samples
Known GenesLOC285692
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16964965
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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