A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629293



Internal ID21577598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15488804..15488804hg38UCSC Ensembl
chr9:15488802..15488802hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161173
SamplesNA12878
Known GenesPSIP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629293
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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