A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862377



Internal ID22637312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72430136..72442138hg38UCSC Ensembl
chr10:74189894..74201896hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3812003
hg1912003
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455732
Samples
Known GenesMICU1, MIR1256
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862377
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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