A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037532



Internal ID92777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72475436..72496371hg38UCSC Ensembl
chr10:74235194..74256129hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3820936
hg1920936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480604
Supporting Variants
Samples
Known GenesMICU1, MIR1256
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037532
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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