A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257726



Internal ID22062336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72596561..72596561hg38UCSC Ensembl
chr9:75211477..75211477hg19UCSC Ensembl
Cytoband9q21.13
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 Variantsnssv17841429
Samples
Known GenesTMC1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257726
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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