A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591893



Internal ID21540471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94438761..94438885hg38UCSC Ensembl
chr9:97201043..97201167hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163757
SamplesHG00512
Known GenesHIATL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591893
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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