A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573453



Internal ID20946524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38261302..38350930hg38UCSC Ensembl
chr6:38229078..38318706hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3889629
hg1989629
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270774
Samples
Known GenesBTBD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573453
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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