A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5547966



Internal ID321759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32069358..32069358hg38UCSC Ensembl
chr4:32070980..32070980hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16948727
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5547966
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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