A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936898



Internal ID21356967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25562270..25562270hg38UCSC Ensembl
chr20:25542906..25542906hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187759
SamplesHG002
Known GenesNINL
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936898
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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