A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857303



Internal ID22632238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36601439..36616892hg38UCSC Ensembl
chr11:36622989..36638442hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3815454
hg1915454
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464324
Samples
Known GenesC11orf74
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857303
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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