A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928877



Internal ID22704122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49344317..49344382hg38UCSC Ensembl
chr15:49636514..49636579hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379772
Samples
Known GenesFAM227B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928877
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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