A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730154



Internal ID21400965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60604530..60613859hg38UCSC Ensembl
chr14:61071248..61080577hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg389330
hg199330
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258257, nssv16257675, nssv16257414, nssv16257258, nssv16256831, nssv16258029, nssv16257691, nssv16257358, nssv16256769, nssv16256326, nssv16257030, nssv16257686
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730154
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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