A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066185



Internal ID21975418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10459289..10459289hg38UCSC Ensembl
chr5:10459401..10459401hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540371
Samples
Known GenesROPN1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066185
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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