A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159835



Internal ID21403645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113333278..113333278hg38UCSC Ensembl
chr9:116095558..116095558hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643381
Supporting Variants
SamplesHG00171
Known GenesWDR31
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159835
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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