A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471813



Internal ID22529705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40881611..40883910hg38UCSC Ensembl
chr15:41173809..41176108hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852156
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471813
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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