A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830796



Internal ID22605731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:88792280..88794005hg38UCSC Ensembl
chr1:89257963..89259688hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg381726
hg191726
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482429, nssv17481917
Samples
Known GenesPKN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830796
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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