A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17838478



Internal ID22022121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41008246..41008246hg38UCSC Ensembl
chr7:41047844..41047844hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6239342
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17838478
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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