A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930835



Internal ID22706108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63891373..63891425hg38UCSC Ensembl
chr15:64183572..64183624hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383281
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930835
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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