A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756877



Internal ID20532737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46762238..46762238hg38UCSC Ensembl
chr4:46764255..46764255hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266075
Samples
Known GenesCOX7B2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756877
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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