A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855747



Internal ID22630682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40312777..40317300hg38UCSC Ensembl
chr11:40334327..40338850hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg384524
hg194524
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462363
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855747
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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