A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11074



Internal ID15192948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:149843353..149894958hg38UCSC Ensembl
Outerchr1:149814920..149866512hg19UCSC Ensembl
Outerchr1:148081544..148133136hg18UCSC Ensembl
Outerchr1:146627993..146679585hg17UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3851606
hg1951593
hg1851593
hg1751593
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7182
Supporting Variants
SamplesNA15510
Known GenesHIST2H2AA3, HIST2H2AA4, HIST2H2AB, HIST2H2AC, HIST2H2BC, HIST2H2BE, HIST2H3A, HIST2H3C, HIST2H4A, HIST2H4B
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv11074
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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