A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744330



Internal ID20520329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4137366..4137592hg38UCSC Ensembl
chr11:4158596..4158822hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287222
Samples
Known GenesRRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744330
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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