A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257681



Internal ID22062291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66016688..66016688hg38UCSC Ensembl
chr9:42504653..42504653hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841227
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257681
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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