A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090972



Internal ID22000205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85917193..85917193hg38UCSC Ensembl
chr11:85628236..85628236hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583767
Samples
Known GenesCCDC83
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090972
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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