A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666086



Internal ID21614391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37210697..37210697hg38UCSC Ensembl
chr21:38582998..38582998hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118907
SamplesHG02492
Known GenesDSCR9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666086
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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