A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582934



Internal ID20956005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57475101..57475846hg38UCSC Ensembl
chr14:57941819..57942564hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38746
hg19746
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237867
Samples
Known GenesC14orf105
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582934
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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