A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649583



Internal ID21597888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110201328..110201328hg38UCSC Ensembl
chr13:110853675..110853675hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092935
SamplesHG02587
Known GenesCOL4A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649583
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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