A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928998



Internal ID22704244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11425513..11425564hg38UCSC Ensembl
chr19:11536334..11536385hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409164
Samples
Known GenesCCDC151
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928998
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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