A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909668



Internal ID22684878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95447028..95448262hg38UCSC Ensembl
chr10:97206785..97208019hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381235
hg191235
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356581
Samples
Known GenesSORBS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909668
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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