A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6258034



Internal ID22062644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201160632..201160632hg38UCSC Ensembl
chr1:201129760..201129760hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17842215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6258034
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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