A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564334



Internal ID20937405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41198166..41249567hg38UCSC Ensembl
chr6:41165904..41217305hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3851402
hg1951402
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271440
Samples
Known GenesTREML2, TREML3P, TREML4, TREML5P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564334
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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