A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593902



Internal ID20966973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92738521..92738744hg38UCSC Ensembl
chr14:93204866..93205089hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237730
Samples
Known GenesLGMN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593902
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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