A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907992



Internal ID22683202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:9399119..9462556hg38UCSC Ensembl
chr7:9438749..9502186hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3863438
hg1963438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445388
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907992
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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