A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17548639



Internal ID21872994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188604568..188604568hg38UCSC Ensembl
chr3:188322356..188322356hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070965
Supporting Variants
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17548639
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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