A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668662



Internal ID21616967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37756590..37756590hg38UCSC Ensembl
chr21:39128893..39128893hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118928
SamplesNA19239
Known GenesKCNJ6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668662
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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