A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593562



Internal ID20966633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103783320..103784576hg38UCSC Ensembl
chr14:104249657..104250913hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381257
hg191257
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230576
Samples
Known GenesPPP1R13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593562
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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