A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625232



Internal ID21573537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68793082..68793082hg38UCSC Ensembl
chr9:71407998..71407998hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162420
SamplesHG00171
Known GenesPIP5K1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625232
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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