A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968199



Internal ID46112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:62128472..62175218hg38UCSC Ensembl
chr5:61424299..61471045hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3846747
hg1946747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456099
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968199
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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