A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580891



Internal ID20953962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94292886..94334032hg38UCSC Ensembl
chr14:94759223..94800369hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3841147
hg1941147
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238370
Samples
Known GenesSERPINA10, SERPINA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580891
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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