A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388084



Internal ID22445954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62359830..62377907hg38UCSC Ensembl
chr15:62652029..62670106hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3818078
hg1918078
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940363
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388084
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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