A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7389



Internal ID15205707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:167159209..167419344hg38UCSC Ensembl
Outerchr6:167572697..167832832hg19UCSC Ensembl
Outerchr6:167492687..167752822hg18UCSC Ensembl
Outerchr6:167543108..167803243hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38260136
hg19260136
hg18260136
hg17260136
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9704, nssv604, nssv603, nssv9703
SamplesNA18507, NA19240
Known GenesTCP10, TCP10L2, 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)nsv7389
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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