A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067813



Internal ID21977046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122841895..122841895hg38UCSC Ensembl
chr4:123763050..123763050hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546414
Samples
Known GenesFGF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067813
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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