A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198741



Internal ID20765781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:104951706..104997039hg38UCSC Ensembl
chr1:105494328..105539661hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3845334
hg1945334
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326944
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198741
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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