A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664315



Internal ID21612620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100479861..100479861hg38UCSC Ensembl
chr13:101132115..101132115hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38247
hg19247
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087600
SamplesHG03486
Known GenesPCCA, PCCA-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664315
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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