A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941753



Internal ID22717183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96992247..96992310hg38UCSC Ensembl
chr15:97535477..97535540hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372887
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941753
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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