A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9731



Internal ID15193247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:144160778..144358266hg38UCSC Ensembl
Outerchr7:143857871..144055359hg19UCSC Ensembl
Outerchr7:143488804..143686292hg18UCSC Ensembl
Outerchr7:143295519..143493007hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38197489
hg19197489
hg18197489
hg17197489
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7411
Supporting Variants
SamplesNA18507
Known GenesARHGEF34P, ARHGEF35, 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)nssv9731
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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