A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946089



Internal ID22721574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43088897..43089227hg38UCSC Ensembl
chr15:43381095..43381425hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384255
Samples
Known GenesUBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946089
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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