A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962662



Internal ID42414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14308675..14308733hg38UCSC Ensembl
chr5:14308784..14308842hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455331
Supporting Variants
Samples
Known GenesTRIO
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962662
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.130285


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