A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6246316



Internal ID22050926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92091671..92091671hg38UCSC Ensembl
chr8:93103899..93103899hg19UCSC Ensembl
Cytoband8q21.3
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 Variantsnssv17839264
Samples
Known GenesRUNX1T1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6246316
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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