A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17859518



Internal ID22043161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88761914..88761914hg38UCSC Ensembl
chr6:89471633..89471633hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6256829
Supporting Variants
Samples
Known GenesRNGTT
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17859518
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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