A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096900



Internal ID22006133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90780470..90780470hg38UCSC Ensembl
chr14:91246814..91246814hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612813
Samples
Known GenesTTC7B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096900
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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