A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066525



Internal ID21975758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55612482..55612482hg38UCSC Ensembl
chr4:56478649..56478649hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541545
Samples
Known GenesNMU
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066525
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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