A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569996



Internal ID20943067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134214482..134215256hg38UCSC Ensembl
chr6:134535620..134536394hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271921
Samples
Known GenesSGK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569996
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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