A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554799



Internal ID327972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38229307..38229358hg38UCSC Ensembl
chr9:38229304..38229355hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024804
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554799
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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