A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256922



Internal ID22061532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99550671..99550671hg38UCSC Ensembl
chr6:99998547..99998547hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17859480
Samples
Known GenesCCNC
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256922
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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