A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749067



Internal ID20525096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154496307..154496503hg38UCSC Ensembl
chr6:154817441..154817637hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272883
Samples
Known GenesCNKSR3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749067
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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