A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864667



Internal ID22639602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27681066..27683365hg38UCSC Ensembl
chr12:27833999..27836298hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv354n209
Supporting Variantsnssv17463889
Samples
Known GenesPPFIBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864667
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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