A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560611



Internal ID20933682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137826077..137827348hg38UCSC Ensembl
chr6:138147214..138148485hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381272
hg191272
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272437
Samples
Known GenesLOC100130476
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560611
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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