A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062323



Internal ID21971556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47997808..47997808hg38UCSC Ensembl
chr4:47999825..47999825hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38535
hg19535
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545114
Samples
Known GenesCNGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062323
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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