A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6239669



Internal ID22044279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122840446..122840446hg38UCSC Ensembl
chr7:122480500..122480500hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17839767
Samples
Known GenesCADPS2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6239669
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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