A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047590



Internal ID20614630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38415064..38422101hg38UCSC Ensembl
chr19:38905704..38912741hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg387038
hg197038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531255
Supporting Variants
Samples
Known GenesRASGRP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047590
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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