A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646036



Internal ID21594341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79146424..79146424hg38UCSC Ensembl
chr18:76906424..76906424hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381584
hg191584
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17102581, nssv17102582
SamplesNA19239, HG00731
Known GenesATP9B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646036
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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