A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591018



Internal ID20964089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45197042..45198537hg38UCSC Ensembl
chr14:45666245..45667740hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg381496
hg191496
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233771
Samples
Known GenesFANCM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591018
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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