A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460321



Internal ID238311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71272647..71309964hg38UCSC Ensembl
chr6:71982350..72019667hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3837318
hg1937318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987174
Samples
Known GenesOGFRL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460321
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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