A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1693



Internal ID15194290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:144176648..144332699hg38UCSC Ensembl
Outerchr7:143873741..144029792hg19UCSC Ensembl
Outerchr7:143504674..143660725hg18UCSC Ensembl
Outerchr7:143311389..143467440hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38156052
hg19156052
hg18156052
hg17156052
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7411
Supporting Variants
SamplesNA18555
Known GenesARHGEF34P, ARHGEF35, CTAGE4, CTAGE8, OR2A1, OR2A20P, OR2A42, OR2A7, 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)nssv1693
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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