A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997698



Internal ID21907041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42903148..42903836hg38UCSC Ensembl
chr4:42905165..42905853hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38689
hg19689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548740
Samples
Known GenesGRXCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997698
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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