A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590230



Internal ID20963301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:50947906..50948693hg38UCSC Ensembl
chr14:51414624..51415411hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38788
hg19788
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229937
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590230
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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