A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041412



Internal ID95313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14546371..14546448hg38UCSC Ensembl
chr11:14567917..14567994hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496083
Supporting Variants
Samples
Known GenesPSMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041412
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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