A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257839



Internal ID22062449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83284102..83284102hg38UCSC Ensembl
chr9:85899017..85899017hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17840846
Samples
Known GenesFRMD3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257839
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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