A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711733



Internal ID135399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15793113..15799688hg38UCSC Ensembl
chr17:15696427..15703002hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg386576
hg196576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526612
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711733
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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