A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088888



Internal ID21998121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93106226..93106226hg38UCSC Ensembl
chr14:93572571..93572571hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg382607
hg192607
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609970
Samples
Known GenesITPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088888
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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