A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203666



Internal ID20770706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:628601..649600hg38UCSC Ensembl
chr1:563981..584980hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3821000
hg1921000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327476
Supporting Variants
Samples
Known GenesMIR6723
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203666
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.16568


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