A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6250599



Internal ID22055209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8428347..8428347hg38UCSC Ensembl
chr17:8331665..8331665hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17848084
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6250599
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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