A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100973



Internal ID20668013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52591763..52591962hg38UCSC Ensembl
chr3:52625779..52625978hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360086
Supporting Variants
Samples
Known GenesPBRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100973
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00093


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