A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586863



Internal ID20959934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112429812..112430085hg38UCSC Ensembl
chr12:112867616..112867889hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233956
Samples
Known GenesPTPN11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586863
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer