A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098145



Internal ID20665185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167728582..167729332hg38UCSC Ensembl
chr3:167446370..167447120hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38751
hg19751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372267
Supporting Variants
Samples
Known GenesPDCD10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098145
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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