A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711666



Internal ID135332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15072380..15104010hg38UCSC Ensembl
chr17:14975697..15007327hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3831631
hg1931631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523921
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711666
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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