A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594942



Internal ID21543544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77391743..77398952hg38UCSC Ensembl
chr13:77965878..77973087hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg387210
hg197210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098694
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594942
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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