A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171633



Internal ID20738673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101426492..101432940hg38UCSC Ensembl
chr9:104188774..104195222hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg386449
hg196449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448081
Supporting Variants
Samples
Known GenesALDOB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171633
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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