A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380166



Internal ID22438036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35190062..35190116hg38UCSC Ensembl
chr15:35482263..35482317hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943686
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380166
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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