A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890701



Internal ID22665729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139348609..139348927hg38UCSC Ensembl
chr5:138684298..138684616hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423619
Samples
Known GenesPAIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890701
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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