A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595056



Internal ID21543658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92872199..92872457hg38UCSC Ensembl
chr9:95634481..95634739hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163255
SamplesHG00731
Known GenesZNF484
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595056
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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