A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16964248



Internal ID43471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35191048..35191369hg38UCSC Ensembl
chr5:35191150..35191471hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467120
Supporting Variants
Samples
Known GenesPRLR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16964248
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.206681


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