A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075460



Internal ID21984693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25184523..25184523hg38UCSC Ensembl
chr4:25186145..25186145hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543497
Samples
Known GenesSEPSECS-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075460
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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