A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601665



Internal ID21550315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79292550..79294753hg38UCSC Ensembl
chr9:81907465..81909668hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg382204
hg192204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162462
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601665
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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