A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488909



Internal ID266204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23473481..23473652hg38UCSC Ensembl
chr7:23513100..23513271hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994514
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488909
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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