A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867301



Internal ID22642236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72495100..72519321hg38UCSC Ensembl
chr10:74254858..74279079hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3824222
hg1924222
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458425
Samples
Known GenesMICU1, MIR1256
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867301
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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