A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930302



Internal ID22705567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14609554..14609888hg38UCSC Ensembl
chr19:14720366..14720700hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399867
Samples
Known GenesCLEC17A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930302
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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