A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940971



Internal ID22716387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14548048..14555330hg38UCSC Ensembl
chr19:14658860..14666142hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg387283
hg197283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391242
Samples
Known GenesTECR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940971
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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