A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714884



Internal ID138550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78760369..78760595hg38UCSC Ensembl
chr17:76756451..76756677hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517064
Supporting Variants
Samples
Known GenesCYTH1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714884
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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