A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943905



Internal ID22719361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45484412..45484569hg38UCSC Ensembl
chr15:45776610..45776767hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374658
Samples
Known GenesSLC30A4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943905
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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