A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937407



Internal ID22712774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50325380..50325523hg38UCSC Ensembl
chr19:50828637..50828780hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400670
Samples
Known GenesKCNC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937407
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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