A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202537



Internal ID20769577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240298539..240318288hg38UCSC Ensembl
chr1:240461839..240481588hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3819750
hg1919750
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333705
Supporting Variants
Samples
Known GenesFMN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202537
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