A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601451



Internal ID21793498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68229772..68229772hg38UCSC Ensembl
chr15:68522110..68522110hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092599
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601451
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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