A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565196



Internal ID20938267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11465241..11465934hg38UCSC Ensembl
chr6:11465474..11466167hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268559
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565196
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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