A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655547



Internal ID21603852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90797290..90797290hg38UCSC Ensembl
chr14:91263634..91263634hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080791
SamplesHG00731
Known GenesTTC7B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655547
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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