A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850995



Internal ID22625930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41104163..41122910hg38UCSC Ensembl
chr11:41125713..41144460hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3818748
hg1918748
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455056
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850995
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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