A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6261172



Internal ID22065782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22813873..22813873hg38UCSC Ensembl
chr7:22853492..22853492hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17860214
Samples
Known GenesTOMM7
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6261172
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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