A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493428



Internal ID21150981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:72938395..72950634hg38UCSC Ensembl
chr13:73512533..73524772hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3812240
hg1912240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012817
Samples
Known GenesPIBF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493428
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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