A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17552803



Internal ID21877158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192063025..192063025hg38UCSC Ensembl
chr3:191780814..191780814hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076173
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17552803
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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