A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257916



Internal ID22062526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94136035..94136035hg38UCSC Ensembl
chr9:96898317..96898317hg19UCSC Ensembl
Cytoband9q22.32
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 Variantsnssv17840915
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257916
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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