A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16966188



Internal ID44773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:25773653..25778275hg38UCSC Ensembl
chr5:25773762..25778384hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg384623
hg194623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467713
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16966188
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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