A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561374



Internal ID20934445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85626990..85628348hg38UCSC Ensembl
chr6:86336708..86338066hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg381359
hg191359
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274827
Samples
Known GenesSYNCRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561374
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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