A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850472



Internal ID22625407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100306896..100317325hg38UCSC Ensembl
chr13:100959150..100969579hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3810430
hg1910430
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466235
Samples
Known GenesPCCA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850472
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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