A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559536



Internal ID20932607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108908930..108909779hg38UCSC Ensembl
chr6:109230133..109230982hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38850
hg19850
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267803
Samples
Known GenesARMC2, ARMC2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559536
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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