A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520901



Internal ID297210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32996532..32996613hg38UCSC Ensembl
chr17:31323550..31323631hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712684
Samples
Known GenesSPACA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520901
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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