A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150597



Internal ID21444600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107716882..107716948hg38UCSC Ensembl
chr9:110479163..110479229hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588108
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150597
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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