A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665799



Internal ID21614105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:19877735..20070170hg38UCSC Ensembl
chr21:21250049..21442483hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38192436
hg19192435
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118368
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665799
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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