A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712801



Internal ID136467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35250432..35254766hg38UCSC Ensembl
chr17:33577451..33581785hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg384335
hg194335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528699
Supporting Variants
Samples
Known GenesSLFN5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712801
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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