A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060618



Internal ID21512708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149817539..149876316hg38UCSC Ensembl
chr1:149789093..149847866hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3858778
hg1958774
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672211
Supporting Variants
Samples
Known GenesHIST2H2AA3, HIST2H2AA4, HIST2H2BC, HIST2H3A, HIST2H3C, HIST2H4A, HIST2H4B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060618
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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