A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906755



Internal ID22681958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73530716..73530850hg38UCSC Ensembl
chr3:73579867..73580001hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424529
Samples
Known GenesPDZRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906755
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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