A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711679



Internal ID135345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15295043..15300789hg38UCSC Ensembl
chr17:15198360..15204106hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg385747
hg195747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5525059
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711679
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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