A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091185



Internal ID22000418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90797290..90797290hg38UCSC Ensembl
chr14:91263634..91263634hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602265
Samples
Known GenesTTC7B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091185
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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