A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17838411



Internal ID22022054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98192957..98192957hg38UCSC Ensembl
chr7:97822269..97822269hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6239494
Supporting Variants
Samples
Known GenesLMTK2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17838411
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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