A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6251692



Internal ID22056302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38447717..38447717hg38UCSC Ensembl
chr1:38913389..38913389hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17850035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6251692
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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