A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066449



Internal ID21975682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39346163..39346163hg38UCSC Ensembl
chr6:39313939..39313939hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565755
Samples
Known GenesKIF6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066449
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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