A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934364



Internal ID22709689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12925713..12926310hg38UCSC Ensembl
chr19:13036527..13037124hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396593
Samples
Known GenesFARSA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934364
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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