A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854925



Internal ID22629860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7420773..7429185hg38UCSC Ensembl
chr11:7442004..7450416hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg388413
hg198413
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451021
Samples
Known GenesSYT9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854925
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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