A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046437



Internal ID20613477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4275997..4289114hg38UCSC Ensembl
chr19:4275994..4289111hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3813118
hg1913118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531988
Supporting Variants
Samples
Known GenesSHD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046437
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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