A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465627



Internal ID22523516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72480677..72491182hg38UCSC Ensembl
chr10:74240435..74250940hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3810506
hg1910506
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862346
Supporting Variants
Samples
Known GenesMICU1, MIR1256
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465627
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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