A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845513



Internal ID22620448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42988800..42996687hg38UCSC Ensembl
chr6:42956538..42964425hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg387888
hg197888
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505792
Samples
Known GenesPPP2R5D
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845513
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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