A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589777



Internal ID21538343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50906590..50906656hg38UCSC Ensembl
chr19:51409846..51409912hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105664
SamplesHG00732
Known GenesKLK4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589777
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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