A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712695



Internal ID136361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33239347..33247368hg38UCSC Ensembl
chr17:31566365..31574386hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg388022
hg198022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5514687
Supporting Variants
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712695
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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