A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5396706



Internal ID176121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32684120..32684139hg38UCSC Ensembl
chr4:32685742..32685761hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16947902
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5396706
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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