A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv603



Internal ID15198583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:167177410..167419344hg38UCSC Ensembl
Outerchr6:167590898..167832832hg19UCSC Ensembl
Outerchr6:167510888..167752822hg18UCSC Ensembl
Outerchr6:167561309..167803243hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38241935
hg19241935
hg18241935
hg17241935
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7389
Supporting Variants
SamplesNA19240
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)nssv603
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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