A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6160



Internal ID15537703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:107378290..107422455hg38UCSC Ensembl
Outerchr7:107018735..107062900hg19UCSC Ensembl
Outerchr7:106805971..106850136hg18UCSC Ensembl
Outerchr7:106612686..106656851hg17UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3844166
hg1944166
hg1844166
hg1744166
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7404
Supporting Variants
SamplesNA12156
Known GenesCOG5
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)nssv6160
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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