A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081122



Internal ID21990355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88010661..88010661hg38UCSC Ensembl
chr14:88477005..88477005hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg382862
hg192862
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602342
Samples
Known GenesGPR65
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081122
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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