A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063766



Internal ID21972999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11117339..11117339hg38UCSC Ensembl
chr6:11117572..11117572hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558118
Samples
Known GenesSMIM13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063766
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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