A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111868



Internal ID22021102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10034917..10034917hg38UCSC Ensembl
chr20:10015565..10015565hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618150
Samples
Known GenesSNAP25-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111868
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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