A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17552116



Internal ID21876471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197786394..197880237hg38UCSC Ensembl
chr3:197513265..197607108hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3893844
hg1993844
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993030
Supporting Variants
Samples
Known GenesLRCH3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17552116
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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