A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065329



Internal ID21511568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42222032..42222032hg38UCSC Ensembl
chr1:42687703..42687703hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619452
Supporting Variants
SamplesNA24385
Known GenesFOXJ3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065329
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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