A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863453



Internal ID22638388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130564390..130569666hg38UCSC Ensembl
chr11:130434285..130439561hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg385277
hg195277
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452458
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863453
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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