A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4447821



Internal ID22113999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98825817..98825894hg38UCSC Ensembl
chr8:99838045..99838122hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764610
Samples
Known GenesSTK3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4447821
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer