A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589



Internal ID15191631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:144259018..144351845hg38UCSC Ensembl
Outerchr7:143956111..144048938hg19UCSC Ensembl
Outerchr7:143587044..143679871hg18UCSC Ensembl
Outerchr7:143393759..143486586hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3892828
hg1992828
hg1892828
hg1792828
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7411
Supporting Variants
SamplesNA12878
Known GenesARHGEF34P, 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)nssv3589
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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