A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962097



Internal ID42030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16785243..16786138hg38UCSC Ensembl
chr5:16785352..16786247hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38896
hg19896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470831
Supporting Variants
Samples
Known GenesMYO10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962097
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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