A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751067



Internal ID20526927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20041126..20041126hg38UCSC Ensembl
chr16:20052448..20052448hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269881
Samples
Known GenesGPR139
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751067
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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