A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589089



Internal ID20962160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67265874..67266375hg38UCSC Ensembl
chr14:67732591..67733092hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2184n223
Supporting Variantsnssv18237466
Samples
Known GenesMPP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589089
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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