A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17860148



Internal ID22043791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156886880..156886880hg38UCSC Ensembl
chr1:156856672..156856672hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6245299
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17860148
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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