A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17860061



Internal ID22043704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137827076..137827076hg38UCSC Ensembl
chr6:138148213..138148213hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257252
Supporting Variants
Samples
Known GenesLOC100130476
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17860061
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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