A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839709



Internal ID22023352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116225181..116225181hg38UCSC Ensembl
chr7:115865235..115865235hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6239616
Supporting Variants
Samples
Known GenesTES
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839709
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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