A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5539819



Internal ID314696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120006967..120006967hg38UCSC Ensembl
chr4:120928122..120928122hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16955138
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5539819
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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