A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370635



Internal ID22596304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60080104..60080104hg38UCSC Ensembl
chr15:60372303..60372303hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969628
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370635
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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