A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1694



Internal ID15194291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:144249939..144340998hg38UCSC Ensembl
Outerchr7:143947032..144038091hg19UCSC Ensembl
Outerchr7:143577965..143669024hg18UCSC Ensembl
Outerchr7:143384680..143475739hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3891060
hg1991060
hg1891060
hg1791060
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7411
Supporting Variants
SamplesNA18555
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)nssv1694
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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