A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6467



Internal ID15190711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:67354560..67385632hg38UCSC Ensembl
Outerchr11:67122031..67153103hg19UCSC Ensembl
Outerchr11:66878607..66909679hg18UCSC Ensembl
Outerchr11:66878607..66909679hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3831073
hg1931073
hg1831073
hg1731073
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7220
Supporting Variants
SamplesNA12156
Known GenesCLCF1, LOC100130987
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)nssv6467
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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