A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104788



Internal ID22014022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94853747..94853844hg38UCSC Ensembl
chr14:95320084..95320181hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611860
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104788
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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