A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385680



Internal ID22443550
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 StatusS
Merged Variantsnsv5940399
Supporting Variants
Samples
Known GenesCPLX3, LMAN1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385680
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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