A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17713000



Internal ID136666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38984421..38988607hg38UCSC Ensembl
chr17:37140674..37144860hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg384187
hg194187
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516720
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17713000
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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