A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17860056



Internal ID22043699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151660625..151660625hg38UCSC Ensembl
chr1:151633101..151633101hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6245263
Supporting Variants
Samples
Known GenesSNX27
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17860056
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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