A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569504



Internal ID21517862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24057529..24075322hg38UCSC Ensembl
chr7:24097148..24114941hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3817794
hg1917794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145487
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569504
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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