A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394411



Internal ID22452281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30037003..30038193hg38UCSC Ensembl
chr19:30527910..30529100hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381191
hg191191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928667
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394411
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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