A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600639



Internal ID21549280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89553407..89850361hg38UCSC Ensembl
chr13:90205661..90502615hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38296955
hg19296955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089051
SamplesHG03009
Known GenesLINC00353
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600639
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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