A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561131



Internal ID20934202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82193091..82193870hg38UCSC Ensembl
chr6:82902808..82903587hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38780
hg19780
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274758
Samples
Known GenesIBTK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561131
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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