A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256727



Internal ID22061337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19491053..19491053hg38UCSC Ensembl
chr1:19817547..19817547hg19UCSC Ensembl
Cytoband1p36.13
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 Variantsnssv17857326
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256727
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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