A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9732



Internal ID15193245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:144226073..144289770hg38UCSC Ensembl
Outerchr7:143923166..143986863hg19UCSC Ensembl
Outerchr7:143554099..143617796hg18UCSC Ensembl
Outerchr7:143360814..143424511hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3863698
hg1963698
hg1863698
hg1763698
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7411
Supporting Variants
SamplesNA18507
Known GenesARHGEF34P, CTAGE4, CTAGE8, OR2A1, OR2A20P, OR2A42, OR2A7, OR2A9P
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)nssv9732
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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