A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392960



Internal ID22450830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3094786..3110146hg38UCSC Ensembl
chr19:3094784..3110144hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3815361
hg1915361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5946338
Supporting Variants
Samples
Known GenesGNA11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392960
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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