A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921486



Internal ID22696710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97089607..97102988hg38UCSC Ensembl
chr9:99851889..99865270hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3813382
hg1913382
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439672
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921486
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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