A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871848



Internal ID22646786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47649417..47651116hg38UCSC Ensembl
chr19:48152674..48154373hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477253
Samples
Known GenesGLTSCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871848
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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