A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650900



Internal ID21599205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77635641..77635641hg38UCSC Ensembl
chr15:77927983..77927983hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090889
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650900
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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