A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062144



Internal ID21971377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185827228..185827228hg38UCSC Ensembl
chr4:186748382..186748382hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543370
Samples
Known GenesSORBS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062144
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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