A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522788



Internal ID299048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35879352..35882137hg38UCSC Ensembl
chr17:34206356..34209141hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg382786
hg192786
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712832
Samples
Known GenesCCL5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522788
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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