A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616509



Internal ID21808556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70130125..70130125hg38UCSC Ensembl
chr15:70422464..70422464hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095927
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616509
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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