A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046058



Internal ID20613098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2668001..2670600hg38UCSC Ensembl
chr19:2667999..2670598hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520255
Supporting Variants
Samples
Known GenesGNG7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046058
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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