A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257947



Internal ID22062557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97483400..97483400hg38UCSC Ensembl
chr9:100245682..100245682hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841094
Samples
Known GenesTDRD7
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257947
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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