A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17548811



Internal ID21873166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188576003..188576003hg38UCSC Ensembl
chr3:188293791..188293791hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076168
Supporting Variants
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17548811
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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