A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17548287



Internal ID21872642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168658854..168658854hg38UCSC Ensembl
chr4:169580005..169580005hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6077178
Supporting Variants
Samples
Known GenesPALLD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17548287
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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