A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098794



Internal ID20665834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:178138607..178139071hg38UCSC Ensembl
chr3:177856395..177856859hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358630
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098794
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00073


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