A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843890



Internal ID22618825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88895329..88898323hg38UCSC Ensembl
chr5:88191146..88194140hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg382995
hg192995
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499536, nssv17500418
Samples
Known GenesMEF2C, MEF2C-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843890
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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