A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028027



Internal ID86379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126476077..126476102hg38UCSC Ensembl
chr9:129238356..129238381hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553570
Supporting Variants
Samples
Known GenesMVB12B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028027
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.128786


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