A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373659



Internal ID22599328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68825347..68825347hg38UCSC Ensembl
chr15:69117686..69117686hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974150
Supporting Variants
Samples
Known GenesMIR548H4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373659
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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