A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046061



Internal ID20613101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2680922..2681754hg38UCSC Ensembl
chr19:2680920..2681752hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532281
Supporting Variants
Samples
Known GenesGNG7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046061
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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