A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100432



Internal ID20667472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180084944..180517871hg38UCSC Ensembl
chr3:179802732..180235659hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38432928
hg19432928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368491
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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