A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17852963



Internal ID22036606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:86348157..86348157hg38UCSC Ensembl
chr2:86575280..86575280hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6252712
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17852963
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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