A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995369



Internal ID21904712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139030037..139030305hg38UCSC Ensembl
chr4:139951191..139951459hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537939
Samples
Known GenesCCRN4L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995369
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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