A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328563



Internal ID20861711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89119239..89129880hg38UCSC Ensembl
chr1:89584922..89595563hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3810642
hg1910642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064908
Samples
Known GenesGBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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