A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570329



Internal ID20943400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38560708..38561498hg38UCSC Ensembl
chr6:38528484..38529274hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270791
Samples
Known GenesBTBD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570329
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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