A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099642



Internal ID20666682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17665510..17946054hg38UCSC Ensembl
chr3:17707002..17987546hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38280545
hg19280545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374633
Supporting Variants
Samples
Known GenesTBC1D5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099642
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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