A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866588



Internal ID22641523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27679466..27683365hg38UCSC Ensembl
chr12:27832399..27836298hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv353n209
Supporting Variantsnssv17464870
Samples
Known GenesPPFIBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866588
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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