A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376470



Internal ID22602139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90926240..90928342hg38UCSC Ensembl
chr15:91469470..91471572hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382103
hg192103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929017
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376470
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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