A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162205



Internal ID21456584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38632765..38633598hg38UCSC Ensembl
chr9:38632762..38633595hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38834
hg19834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601837
Supporting Variants
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162205
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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