A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571784



Internal ID20944855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104239751..104264743hg38UCSC Ensembl
chr6:104687626..104712618hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3824993
hg1924993
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271028
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571784
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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