A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558197



Internal ID20931268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26012786..26023140hg38UCSC Ensembl
chr6:26013014..26023368hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3810355
hg1910355
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270915
Samples
Known GenesHIST1H1A, HIST1H3A, HIST1H4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558197
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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