A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17860120



Internal ID22043763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146076157..146076157hg38UCSC Ensembl
chr6:146397293..146397293hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257306
Supporting Variants
Samples
Known GenesGRM1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17860120
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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