A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9703



Internal ID15193412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:167159209..167359890hg38UCSC Ensembl
Outerchr6:167572697..167773378hg19UCSC Ensembl
Outerchr6:167492687..167693368hg18UCSC Ensembl
Outerchr6:167543108..167743789hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38200682
hg19200682
hg18200682
hg17200682
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7389
Supporting Variants
SamplesNA18507
Known GenesTCP10L2, 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)nssv9703
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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