A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046267



Internal ID20613307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35016313..35016616hg38UCSC Ensembl
chr19:35507217..35507520hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529682
Supporting Variants
Samples
Known GenesGRAMD1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046267
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