A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529122



Internal ID20902483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13674683..13676333hg38UCSC Ensembl
chr18:13674682..13676332hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381651
hg191651
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186571
Samples
Known GenesFAM210A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529122
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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