A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913619



Internal ID22688835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134190878..134190945hg38UCSC Ensembl
chr7:133875630..133875697hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437479
Samples
Known GenesLRGUK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913619
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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