A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007634



Internal ID6712128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:149800570..149882044hg38UCSC Ensembl
Outerchr1:149772126..149853594hg19UCSC Ensembl
Outerchr1:148038750..148120218hg18UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3881475
hg1981469
hg1881469
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564759
SamplesHuRef
Known GenesHIST2H2AA3, HIST2H2AA4, HIST2H2BC, HIST2H2BF, HIST2H3A, HIST2H3C, HIST2H3D, HIST2H4A, HIST2H4B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007634
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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