A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607799



Internal ID21799846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94767635..94767635hg38UCSC Ensembl
chr15:95310864..95310864hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084542
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607799
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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