A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656935



Internal ID21605240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77643065..77643065hg38UCSC Ensembl
chr15:77935407..77935407hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg383435
hg193435
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084253
SamplesHG03065
Known GenesLOC253044
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656935
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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