A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618212



Internal ID21810259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76073501..76073501hg38UCSC Ensembl
chr17:74069582..74069582hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg382920
hg192920
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085464
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618212
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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