A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981752



Internal ID21891095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:170689814..170689870hg38UCSC Ensembl
chr1:170658955..170659011hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533302
Samples
Known GenesPRRX1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981752
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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