A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594785



Internal ID21543385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91073294..91073430hg38UCSC Ensembl
chr9:93835576..93835712hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163385
SamplesHG02818
Known GenesLOC100129316
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594785
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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