A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633147



Internal ID21581452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97362666..97362666hg38UCSC Ensembl
chr9:100124948..100124948hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163419
SamplesHG02587
Known GenesCCDC180, LOC100499484-C9ORF174
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633147
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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