A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17160295



Internal ID21427713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128464665..128464860hg38UCSC Ensembl
chr9:131226944..131227139hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590897
Supporting Variants
SamplesHG00731
Known GenesODF2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17160295
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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