A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671672



Internal ID21619978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14980613..14980613hg38UCSC Ensembl
chr21:16352934..16352934hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118238
SamplesNA19238
Known GenesNRIP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671672
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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