A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487338



Internal ID264678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126376631..126378377hg38UCSC Ensembl
chr9:129138910..129140656hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381747
hg191747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738538
Samples
Known GenesMVB12B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487338
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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