A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942431



Internal ID22717868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82965866..83024030hg38UCSC Ensembl
chr15:83634618..83692782hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3858165
hg1958165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370653
Samples
Known GenesBTBD1, C15orf40, FAM103A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942431
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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