A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467191



Internal ID245010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14994870..15494944hg38UCSC Ensembl
chr7:15034495..15534569hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38500075
hg19500075
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16993477
Samples
Known GenesAGMO
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467191
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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