A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17548836



Internal ID21873191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155938940..155938940hg38UCSC Ensembl
chr3:155656729..155656729hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg381180
hg191180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6066760
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17548836
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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