A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201056



Internal ID20768096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175057101..175126400hg38UCSC Ensembl
chr1:175026237..175095536hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3869300
hg1969300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320981
Supporting Variants
Samples
Known GenesTNN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201056
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00795


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer