A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577130



Internal ID20950201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37162484..37951101hg38UCSC Ensembl
chr14:37631689..38420306hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38788618
hg19788618
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231666
Samples
Known GenesFOXA1, MIPOL1, SLC25A21, SLC25A21-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577130
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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