A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940975



Internal ID22716391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74454852..74455001hg38UCSC Ensembl
chr15:74747193..74747342hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378136
Samples
Known GenesUBL7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940975
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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