A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575988



Internal ID21524422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45788758..45788836hg38UCSC Ensembl
chr7:45828357..45828435hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153873
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575988
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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