A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569032



Internal ID20942103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34788473..34789559hg38UCSC Ensembl
chr6:34756250..34757336hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381087
hg191087
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271255
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569032
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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