A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757842



Internal ID20533702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3358759..3358759hg38UCSC Ensembl
chr11:3379989..3379989hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288576
Samples
Known GenesZNF195
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757842
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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