A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757761



Internal ID20533621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10501876..10501876hg38UCSC Ensembl
chr11:10523423..10523423hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381517
hg191517
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269476
Samples
Known GenesAMPD3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757761
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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