A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945780



Internal ID22721261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7749994..7759445hg38UCSC Ensembl
chr19:7814880..7824331hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg389452
hg199452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401120
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945780
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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