A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159855



Internal ID21407220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113900833..113900949hg38UCSC Ensembl
chr9:116663113..116663229hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598928
Supporting Variants
SamplesHG00512
Known GenesZNF618
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159855
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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