A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077178



Internal ID21986411
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 StatusM
Merged Variants
Supporting Variantsnssv17548287
Samples
Known GenesPALLD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077178
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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