A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589117



Internal ID21537681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100550321..100550416hg38UCSC Ensembl
chr13:101202575..101202670hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082190
SamplesNA19239
Known GenesGGACT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589117
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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