A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549883



Internal ID21874238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168499319..168499319hg38UCSC Ensembl
chr4:169420470..169420470hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6062212
Supporting Variants
Samples
Known GenesPALLD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549883
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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