A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845633



Internal ID22620568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5085896..5086895hg38UCSC Ensembl
chr6:5086130..5087129hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506440
Samples
Known GenesPPP1R3G
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845633
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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