A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837324



Internal ID22612259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118704340..118743849hg38UCSC Ensembl
chr4:119625495..119665004hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3839510
hg1939510
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492286
Samples
Known GenesMETTL14, SEC24D
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837324
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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