A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659096



Internal ID21607401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85896996..85896996hg38UCSC Ensembl
chr15:86440227..86440227hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081477
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659096
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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