A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651220



Internal ID21599525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97641169..97641169hg38UCSC Ensembl
chr15:98184399..98184399hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098365
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651220
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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