A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256641



Internal ID22061251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10214028..10214028hg38UCSC Ensembl
chr6:10214261..10214261hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17858755
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256641
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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