A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199866



Internal ID20766906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205468496..205487733hg38UCSC Ensembl
chr1:205437624..205456861hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3819238
hg1919238
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316539
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199866
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00048


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