A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052866



Internal ID20619906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:166123027..166125502hg38UCSC Ensembl
chr1:166092264..166094739hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg382476
hg192476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326935
Supporting Variants
Samples
Known GenesFAM78B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052866
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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