A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456366



Internal ID234436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22771134..22775845hg38UCSC Ensembl
chr7:22810753..22815464hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg384712
hg194712
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16993206
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456366
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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