A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908231



Internal ID22683441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81799735..81806482hg38UCSC Ensembl
chr9:84414650..84421397hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg386748
hg196748
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908231
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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