A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851061



Internal ID22625996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72453719..72472957hg38UCSC Ensembl
chr10:74213477..74232715hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3819239
hg1919239
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465326
Samples
Known GenesMICU1, MIR1256
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851061
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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