A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934539



Internal ID22709867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95781658..95802557hg38UCSC Ensembl
chr15:96324887..96345786hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3820900
hg1920900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388953
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934539
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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