A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072553



Internal ID21981786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41029766..41029766hg38UCSC Ensembl
chr6:40997505..40997505hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576876
Samples
Known GenesUNC5CL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072553
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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