A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17838538



Internal ID22022181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46400780..46400780hg38UCSC Ensembl
chr7:46440378..46440378hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6239391
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17838538
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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