A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047219



Internal ID20614259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15016041..15025062hg38UCSC Ensembl
chr19:15126853..15135874hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg389022
hg199022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530433
Supporting Variants
Samples
Known GenesCCDC105
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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