A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1921



Internal ID15194518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1884017..1910630hg38UCSC Ensembl
Outerchr11:1905247..1931860hg19UCSC Ensembl
Outerchr11:1861823..1888436hg18UCSC Ensembl
Outerchr11:1861823..1888436hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3826614
hg1926614
hg1826614
hg1726614
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7213
Supporting Variants
SamplesNA18555
Known GenesLSP1
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)nssv1921
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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