A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17379772



Internal ID22437642
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 StatusS
Merged Variantsnsv5928877
Supporting Variants
Samples
Known GenesFAM227B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17379772
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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