A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656123



Internal ID21604428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77460457..77460457hg38UCSC Ensembl
chr14:77926800..77926800hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091522
SamplesHG00731
Known GenesAHSA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656123
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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