A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940047



Internal ID22715450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90675943..90679564hg38UCSC Ensembl
chr15:91219174..91222795hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383622
hg193622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372164
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940047
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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