A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17387725



Internal ID22445595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57692633..57693594hg38UCSC Ensembl
chr15:57984831..57985792hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38962
hg19962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943366
Supporting Variants
Samples
Known GenesGCOM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17387725
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002


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