A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6250322



Internal ID22054932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57628720..57628720hg38UCSC Ensembl
chr16:57662632..57662632hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17847270
Samples
Known GenesGPR56
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6250322
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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