A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563335



Internal ID20936406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139036959..139037051hg38UCSC Ensembl
chr6:139358096..139358188hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272485
Samples
Known GenesABRACL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563335
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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