A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562847



Internal ID20935918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95421299..95428049hg38UCSC Ensembl
chr6:95869175..95875925hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg386751
hg196751
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272182
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562847
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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