A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202112



Internal ID20769152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96013541..96034671hg38UCSC Ensembl
chr1:96479097..96500227hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3821131
hg1921131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317018
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202112
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