A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560898



Internal ID20933969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107712658..107714980hg38UCSC Ensembl
chr6:108033862..108036184hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382323
hg192323
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269218
Samples
Known GenesSCML4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560898
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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