A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933277



Internal ID21353346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42277506..42277821hg38UCSC Ensembl
chr1:42743177..42743492hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15182826
SamplesHG002
Known GenesFOXJ3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3933277
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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