A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18004852



Internal ID20571893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:89447019..89484229hg38UCSC Ensembl
chr12:89840796..89878006hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3837211
hg1937211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460970
Supporting Variants
Samples
Known GenesPOC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18004852
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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