A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940399



Internal ID22715807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74823435..74833001hg38UCSC Ensembl
chr15:75115776..75125342hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg389567
hg199567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385680
Samples
Known GenesCPLX3, LMAN1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940399
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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