A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712832



Internal ID136498
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 StatusS
Merged Variantsnsv5522788
Supporting Variants
Samples
Known GenesCCL5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712832
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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