A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590302



Internal ID21538871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100458545..100458594hg38UCSC Ensembl
chr9:103220827..103220876hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149367
SamplesHG00731
Known GenesMSANTD3-TMEFF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590302
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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