A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257297



Internal ID22061907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144840725..144840725hg38UCSC Ensembl
chr6:145161861..145161861hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17860110
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257297
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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