A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691



Internal ID15198621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:144210990..144379150hg38UCSC Ensembl
Outerchr7:143908083..144076243hg19UCSC Ensembl
Outerchr7:143539016..143707176hg18UCSC Ensembl
Outerchr7:143345731..143513891hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38168161
hg19168161
hg18168161
hg17168161
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7411
Supporting Variants
SamplesNA19240
Known GenesARHGEF34P, ARHGEF5, 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)nssv691
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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