A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097759



Internal ID20664799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181107441..181111492hg38UCSC Ensembl
chr3:180825229..180829280hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg384052
hg194052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360186
Supporting Variants
Samples
Known GenesSOX2-OT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097759
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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