A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162938



Internal ID21506929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87060411..87068095hg38UCSC Ensembl
chr9:89675326..89683010hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg387685
hg197685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601310
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162938
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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