A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996131



Internal ID21905474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185240314..185240443hg38UCSC Ensembl
chr4:186161468..186161597hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545235
Samples
Known GenesSNX25
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996131
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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