A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161785



Internal ID21451864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40506558..40508954hg38UCSC Ensembl
chr9:42848005..42850402hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg382397
hg192398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596263
Supporting Variants
SamplesHG01596
Known GenesLOC286297
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161785
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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