A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913312



Internal ID22688528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83049519..83055591hg38UCSC Ensembl
chr9:85664434..85670506hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg386073
hg196073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439993
Samples
Known GenesRASEF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913312
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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