A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925354



Internal ID22700581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72429875..72588406hg38UCSC Ensembl
chr10:74189633..74348164hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38158532
hg19158532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357814
Samples
Known GenesMICU1, MIR1256
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925354
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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