A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555574



Internal ID328728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110253386..110253437hg38UCSC Ensembl
chr9:113015666..113015717hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38880
hg19880
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026801
Samples
Known GenesTXN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555574
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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