A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579713



Internal ID20952784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:29534751..29535509hg38UCSC Ensembl
chr14:30003957..30004715hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38759
hg19759
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227673
Samples
Known GenesMIR548AI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579713
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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