A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607749



Internal ID21799796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69045552..69045552hg38UCSC Ensembl
chr15:69337892..69337892hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6089810
Supporting Variants
Samples
Known GenesMIR548H4, NOX5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607749
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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