A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586607



Internal ID20959678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81347505..81350654hg38UCSC Ensembl
chr14:81813849..81816998hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg383150
hg193150
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238209
Samples
Known GenesSTON2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586607
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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