A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075096



Internal ID21984329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25845697..25845697hg38UCSC Ensembl
chr4:25847319..25847319hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542740
Samples
Known GenesSEL1L3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075096
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer