A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588798



Internal ID20961869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103146408..103249499hg38UCSC Ensembl
chr14:103612745..103715836hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38103092
hg19103092
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227793
Samples
Known GenesLINC00605
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588798
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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