A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6252730



Internal ID22057340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42679749..42679749hg38UCSC Ensembl
chr1:43145420..43145420hg19UCSC Ensembl
Cytoband1p34.2
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 Variantsnssv17852271
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6252730
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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