A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668202



Internal ID21616507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44946309..44946309hg38UCSC Ensembl
chr21:46366224..46366224hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119397
SamplesHG03125
Known GenesFAM207A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668202
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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