A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104871



Internal ID22014104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34547864..34562448hg38UCSC Ensembl
chr14:35017070..35031654hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3814585
hg1914585
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600062
Samples
Known GenesSNX6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104871
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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