A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9704



Internal ID15193403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:167197684..167394676hg38UCSC Ensembl
Outerchr6:167611172..167808164hg19UCSC Ensembl
Outerchr6:167531162..167728154hg18UCSC Ensembl
Outerchr6:167581583..167778575hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38196993
hg19196993
hg18196993
hg17196993
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7389
Supporting Variants
SamplesNA18507
Known GenesTCP10, TTLL2, UNC93A
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)nssv9704
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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