A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959131



Internal ID22734171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54169924..54169924hg38UCSC Ensembl
chr4:55036091..55036091hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959131
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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