A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601835



Internal ID21793882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74991066..74991066hg38UCSC Ensembl
chr15:75283407..75283407hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6096181
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601835
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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