A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380571



Internal ID22438441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84916208..84916490hg38UCSC Ensembl
chr15:85459439..85459721hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942226
Supporting Variants
Samples
Known GenesSLC28A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380571
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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