A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583017



Internal ID20956088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55034141..55034866hg38UCSC Ensembl
chr14:55500859..55501584hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38726
hg19726
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237801
Samples
Known GenesSOCS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583017
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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