A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199885



Internal ID20766925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206563736..206575443hg38UCSC Ensembl
chr1:206737064..206748770hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3811708
hg1911707
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320512
Supporting Variants
Samples
Known GenesRASSF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199885
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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