A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012460



Internal ID21921803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135300146..135300200hg38UCSC Ensembl
chr5:134635836..134635890hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550552
Samples
Known GenesC5orf66
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012460
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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