A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594995



Internal ID21543597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135548993..135549056hg38UCSC Ensembl
chr9:138440839..138440902hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160534
SamplesHG03125
Known GenesOBP2A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594995
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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