A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497902



Internal ID22555836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86155426..86217467hg38UCSC Ensembl
chr4:87076579..87138620hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3862042
hg1962042
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839838
Supporting Variants
Samples
Known GenesMAPK10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497902
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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