A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595302



Internal ID21543906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109356630..109361831hg38UCSC Ensembl
chr9:112118910..112124111hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg385202
hg195202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153025
SamplesHG00514
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595302
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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