A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145781



Internal ID21421492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107255996..107258566hg38UCSC Ensembl
chr9:110018277..110020847hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382571
hg192571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584649
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145781
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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