A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257707



Internal ID22062317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70309349..70309349hg38UCSC Ensembl
chr9:72924265..72924265hg19UCSC Ensembl
Cytoband9q21.12
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 Variantsnssv17841412
Samples
Known GenesSMC5
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257707
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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