A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712689



Internal ID136355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33067989..33068464hg38UCSC Ensembl
chr17:31395007..31395482hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522531
Supporting Variants
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712689
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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