A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519943



Internal ID20893304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1999697..2001362hg38UCSC Ensembl
chr19:1999696..2001361hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381666
hg191666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045471
Samples
Known GenesBTBD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519943
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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