A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898937



Internal ID22674061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139355392..139359358hg38UCSC Ensembl
chr5:138691081..138695047hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg383967
hg193967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426845
Samples
Known GenesPAIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898937
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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