A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18045138



Internal ID20612178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16910079..16911881hg38UCSC Ensembl
chr19:17020889..17022691hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381803
hg191803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530354
Supporting Variants
Samples
Known GenesCPAMD8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18045138
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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