A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603272



Internal ID21551935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31440562..31440691hg38UCSC Ensembl
chr13:32014699..32014828hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092198
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5603272
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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