A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738399



Internal ID20514367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47006501..47012134hg38UCSC Ensembl
chr11:47028052..47033685hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg385634
hg195634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264868
Samples
Known GenesC11orf49
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738399
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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