A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259069



Internal ID22063679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75159382..75159382hg38UCSC Ensembl
chr17:73155477..73155477hg19UCSC 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 Variantsnssv17849016
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259069
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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