A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6253200



Internal ID22057810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:196816226..196816226hg38UCSC Ensembl
chr2:197680950..197680950hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17853377
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6253200
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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