A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593004



Internal ID21541589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126484619..126484943hg38UCSC Ensembl
chr9:129246898..129247222hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159738
SamplesHG00731
Known GenesMVB12B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593004
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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