A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559144



Internal ID332188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:7814388..7814439hg38UCSC Ensembl
chr9:7814388..7814439hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021058
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559144
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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