A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046062



Internal ID20613102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2683001..2684900hg38UCSC Ensembl
chr19:2682999..2684898hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532241
Supporting Variants
Samples
Known GenesGNG7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046062
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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