A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937428



Internal ID22712795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67242127..67242460hg38UCSC Ensembl
chr15:67534465..67534798hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379698
Samples
Known GenesAAGAB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937428
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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