A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935314



Internal ID22710653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92571415..92571493hg38UCSC Ensembl
chr15:93114645..93114723hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385079
Samples
Known GenesLINC00930
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935314
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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