A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644930



Internal ID21593235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105502114..105502114hg38UCSC Ensembl
chr14:105968451..105968451hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092044
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644930
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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