A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933032



Internal ID21353101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21693782..21693782hg38UCSC Ensembl
chr8:21551294..21551294hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204041
SamplesHG002
Known GenesGFRA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3933032
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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