A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916495



Internal ID22691714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45789812..45789879hg38UCSC Ensembl
chr10:46285260..46285327hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355183
Samples
Known GenesFAM21C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916495
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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