A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517436



Internal ID20890797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4012161..4019521hg38UCSC Ensembl
chr18:4012161..4019521hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg387361
hg197361
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188844
Samples
Known GenesDLGAP1, DLGAP1-AS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517436
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