A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976102



Internal ID22751037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42014394..42014394hg38UCSC Ensembl
chr21:43434503..43434503hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406283
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976102
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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