A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199240



Internal ID20766280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109206267..109215956hg38UCSC Ensembl
chr1:109748889..109758578hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg389690
hg199690
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327238
Supporting Variants
Samples
Known GenesKIAA1324, SARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199240
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00132


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