A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667336



Internal ID21615642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150154235..150168703hg38UCSC Ensembl
chr6:150475371..150489839hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3814469
hg1914469
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157998
Samples
Known GenesPPP1R14C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667336
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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