A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051768



Internal ID21961001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10071990..10072050hg38UCSC Ensembl
chr19:10182666..10182726hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619075
Samples
Known GenesC3P1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051768
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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