A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764591



Internal ID20540451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88980179..88980179hg38UCSC Ensembl
chr10:90739936..90739936hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274070
Samples
Known GenesACTA2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764591
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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