A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145828



Internal ID345033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45205072..45209902hg38UCSC Ensembl
chr17:43282439..43287269hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg384831
hg194831
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17713356
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145828
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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