A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083349



Internal ID21461131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75629499..75629499hg38UCSC Ensembl
chr14:76095842..76095842hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646350
Supporting Variants
SamplesHG02818
Known GenesFLVCR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083349
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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