A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064886



Internal ID20631926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:88835858..88836448hg38UCSC Ensembl
chr1:89301541..89302131hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323759
Supporting Variants
Samples
Known GenesPKN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064886
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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