A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578971



Internal ID20952042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30892832..30893037hg38UCSC Ensembl
chr14:31362038..31362243hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231415
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578971
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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