A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712758



Internal ID136424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34409810..34409996hg38UCSC Ensembl
chr17:32736829..32737015hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516685
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712758
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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