A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097162



Internal ID21500450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103051149..103051149hg38UCSC Ensembl
chr14:103517486..103517486hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658034
Supporting Variants
SamplesNA19239
Known GenesCDC42BPB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097162
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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