A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452347



Internal ID22510220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60955646..60956769hg38UCSC Ensembl
chr10:62715404..62716527hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg381124
hg191124
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850316
Supporting Variants
Samples
Known GenesRHOBTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452347
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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