A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17852491



Internal ID22036134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105256770..105256770hg38UCSC Ensembl
chr2:105873227..105873227hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6252809
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17852491
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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