A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048055



Internal ID20615095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41118165..41120169hg38UCSC Ensembl
chr19:41624070..41626074hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382005
hg192005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524921
Supporting Variants
Samples
Known GenesCYP2F1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048055
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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