A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456444



Internal ID234511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:31864754..31883423hg38UCSC Ensembl
chr5:31864860..31883529hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3818670
hg1918670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16964140
Samples
Known GenesPDZD2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456444
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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