A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568372



Internal ID20941443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21391567..22908554hg38UCSC Ensembl
chr6:21391798..22908783hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381516988
hg191516986
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270195
Samples
Known GenesCASC14, CASC15, HDGFL1, LINC00581, PRL, SOX4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568372
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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