A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17550431



Internal ID21874786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76549425..76551905hg38UCSC Ensembl
chr4:77470578..77473058hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg382481
hg192481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5998593
Supporting Variants
Samples
Known GenesSHROOM3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17550431
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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