A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17851094



Internal ID22034737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203376753..203376753hg38UCSC Ensembl
chr2:204241476..204241476hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253264
Supporting Variants
Samples
Known GenesABI2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17851094
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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