A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1527



Internal ID15198866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:149801682..149850045hg38UCSC Ensembl
Outerchr1:149773238..149821612hg19UCSC Ensembl
Outerchr1:148039862..148088236hg18UCSC Ensembl
Outerchr1:146586311..146634685hg17UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3848364
hg1948375
hg1848375
hg1748375
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7182
Supporting Variants
SamplesNA19240
Known GenesHIST2H2AA3, HIST2H2AA4, HIST2H2BF, HIST2H3A, HIST2H3C, HIST2H3D, 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)nssv1527
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer