A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3587



Internal ID15191629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:144229637..144363508hg38UCSC Ensembl
Outerchr7:143926730..144060601hg19UCSC Ensembl
Outerchr7:143557663..143691534hg18UCSC Ensembl
Outerchr7:143364378..143498249hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38133872
hg19133872
hg18133872
hg17133872
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7411
Supporting Variants
SamplesNA12878
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)nssv3587
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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