A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259059



Internal ID22063669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73651167..73651167hg38UCSC Ensembl
chr17:71647306..71647306hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17849006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259059
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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