A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5599457



Internal ID21548091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121642009..121642064hg38UCSC Ensembl
chr9:124404288..124404343hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159866
SamplesHG00512
Known GenesDAB2IP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5599457
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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