A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579739



Internal ID21528220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45808843..45810711hg38UCSC Ensembl
chr7:45848442..45850310hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg381869
hg191869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147735
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579739
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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