A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257352



Internal ID22061962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151637550..151637550hg38UCSC Ensembl
chr6:151958685..151958685hg19UCSC Ensembl
Cytoband6q25.1
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 Variantsnssv17859882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257352
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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