A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046315



Internal ID20613355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3590503..3590871hg38UCSC Ensembl
chr19:3590501..3590869hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517484
Supporting Variants
Samples
Known GenesGIPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046315
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00074


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