A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741500



Internal ID20517477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134190900..134191098hg38UCSC Ensembl
chr7:133875652..133875850hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285578
Samples
Known GenesLRGUK
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741500
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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