A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162180



Internal ID21485564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38075800..38075959hg38UCSC Ensembl
chr9:38075797..38075956hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596718
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162180
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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