A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937890



Internal ID21357959
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 Variantsnssv15199083
SamplesHG002
Known GenesSTK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937890
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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