A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099939



Internal ID20666979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43011910..43012914hg38UCSC Ensembl
chr3:43053402..43054406hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg381005
hg191005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368077
Supporting Variants
Samples
Known GenesFAM198A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099939
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00427


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