A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1941



Internal ID15194538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:62095114..62141019hg38UCSC Ensembl
Outerchr11:61862586..61908491hg19UCSC Ensembl
Outerchr11:61619162..61665067hg18UCSC Ensembl
Outerchr11:61619162..61665067hg17UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3845906
hg1945906
hg1845906
hg1745906
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7219
Supporting Variants
SamplesNA18555
Known GenesINCENP
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)nssv1941
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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