A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6245829



Internal ID22050439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32179214..32179214hg38UCSC Ensembl
chr8:32036730..32036730hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17839168
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6245829
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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