A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5029



Internal ID15196175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:144262616..144345228hg38UCSC Ensembl
Outerchr7:143959709..144042321hg19UCSC Ensembl
Outerchr7:143590642..143673254hg18UCSC Ensembl
Outerchr7:143397357..143479969hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3882613
hg1982613
hg1882613
hg1782613
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7411
Supporting Variants
SamplesNA19129
Known GenesARHGEF34P, CTAGE4, CTAGE8, OR2A1, OR2A20P, OR2A42, OR2A9P, RNU6-57P
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)nssv5029
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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