A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481917



Internal ID22539822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:88792280..88794005hg38UCSC Ensembl
chr1:89257963..89259688hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg381726
hg191726
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830796
Supporting Variants
Samples
Known GenesPKN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481917
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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