A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559101



Internal ID20932172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5965372..5966628hg38UCSC Ensembl
chr6:5965605..5966861hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg381257
hg191257
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6051n223
Supporting Variantsnssv18271611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559101
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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