A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631664



Internal ID21579969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127834296..127834296hg38UCSC Ensembl
chr9:130596575..130596575hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159918
SamplesHG00864
Known GenesENG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631664
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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