A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050721



Internal ID21959954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15362874..15362952hg38UCSC Ensembl
chr19:15473685..15473763hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630485
Samples
Known GenesAKAP8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050721
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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