A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712775



Internal ID136441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34788884..34795139hg38UCSC Ensembl
chr17:33115903..33122158hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg386256
hg196256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526542
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712775
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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