A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946968



Internal ID21367039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31713725..31714078hg38UCSC Ensembl
chr8:31571241..31571594hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15198741
SamplesHG002
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946968
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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