A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046244



Internal ID20613284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3467701..3474700hg38UCSC Ensembl
chr19:3467699..3474698hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523131
Supporting Variants
Samples
Known GenesC19orf77, NFIC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046244
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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