A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843889



Internal ID22618824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88855510..88857309hg38UCSC Ensembl
chr5:88151327..88153126hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500415, nssv17499530
Samples
Known GenesMEF2C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843889
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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